Informational trade publication · B2B only All figures indicative, as of 2026

Informational trade publication — no medical claims, no consumer sales

Bali Kratom Export · trade intelligence

Bali kratom export intelligence for European B2B buyers

A compliance-desk briefing on the full provenance-to-port line — from West Kalimantan smallholder leaf through Bali GMP processing, accredited lab assay, HS classification and EU port of entry to the member-state legality gate. Every figure date-stamped, indicative, and built for your compliance team to verify. This is a Bali kratom export reference, not a shop.

6 Stations, farm to port
11 Parameters in the assay panel
100 Questions answered in the FAQ
2026 All figures indicative, as of

The custom feature

The Consignment Passport

Choose three inputs. We assemble a date-stamped batch passport card — the required lab-assay panel, Indonesian export document set, indicative quality-spec band, suggested Incoterm and route, and a member-state legality plus EU novel-food note. Reproducible, honest, and framed for your compliance team.

1 · Product form
2 · EU destination market
3 · Order tier

Batch Passport · indicative, as of 2026

Dried whole leaf → Germany → Sample & trial

Lab assay panel
Mitragynine & 7-OH by HPLC · heavy metals (Pb, As, Cd, Hg) by ICP-MS · total plate count, yeast & mould, E. coli, Salmonella · moisture.
Document set
Farm origin & batch record · processing & QA record · Certificate of Analysis · PEB & HS-heading note · phytosanitary certificate.
Quality spec band
Mitragynine ~1.2–1.8% · moisture ≤10% · whole / cut leaf · green, low stem.
Incoterm & route
Air from CGK Jakarta to an EU gateway, ~3–7 days indicative. EXW or FOB typical at this size; courier documentation applies.
Legality note
Germany: restricted — informational. Not authorised as a novel food EU-wide; verify with the competent authority.

Informational only — verify every figure with the competent authority. No prices invented, no medical benefit stated.

Select any input to assemble the passport card. The lab panel, document checklist, spec band, route and legality note are composed for your exact combination.

What the desk holds

Graded, sealed and documented before anything is quoted

A consignment is only as good as the paperwork that travels with it. Stock is graded against a written specification, sealed in food-grade liners, and logged against the lot that produced it before a single figure reaches a quotation.

That is the whole point of the passport: by the time your compliance team opens the file, the origin lot, the assay, the HS line and the member-state position are already in one place and already dated.

  • Lot-level traceability back to the West Kalimantan collection point
  • Specification agreed in writing before production, not after
  • Retained samples held against every shipped lot
  • Assay and heavy-metal results issued by an accredited laboratory

Indicative and as of 2026. Specifications and tolerances are written into the supply contract — verify every figure against your own counsel before you commit.

Graded and sealed stock awaiting dispatch

Graded stock held against its retained sample.

The green provenance line

Provenance to port — six stations, six documents

Every consignment travels the same line. Each station produces the record your customs broker and compliance team will ask for.

  1. West Kalimantan leaf

    Smallholder harvest and origin logging.

    Doc farm origin & batch record

    Origin regions
  2. Bali GMP processing

    Drying, milling and sanitation under GMP-grade controls.

    Doc processing & QA record

    GMP processing
  3. Accredited lab assay

    Alkaloid, heavy-metal and microbial testing.

    Doc Certificate of Analysis (COA)

    Lab testing
  4. HS / customs

    HS-heading classification and export declaration.

    Doc PEB & HS-heading note

    Customs clearance
  5. EU port of entry

    Rotterdam / Hamburg discharge and import clearance.

    Doc import compliance file

    Shipping & routes
  6. Member-state gate

    Destination legality and novel-food status check.

    Doc legality verification note

    EU legality

Plates — the line in photographs

Six stages a buyer can audit

The same six stages the stations above describe in writing. Each plate is a stage a buyer can audit, and each is a point where a consignment is accepted or rejected.

Hand harvesting leaf on an Indonesian smallholding
01

Origin — West Kalimantan leaf

Smallholder collection in the Kapuas basin. The lot number a buyer eventually reads on the certificate is assigned here, not later.

Dried leaf sample weighed out in a porcelain bowl
02

Drying and grading

Leaf is dried to a contracted moisture band and graded against a written specification. Off-spec material leaves the line at this point.

Finely milled botanical powder on a laboratory spoon
03

Milling and GMP processing

Milling to the agreed particle size under a GMP-grade regime, with the 600-micron export rule applied where the destination requires it.

Analyst reading a sample at a laboratory microscope
04

Accredited laboratory assay

Alkaloid profile, heavy metals and microbial safety, issued by an accredited laboratory against the methods named in the contract.

Export documentation assembled on a desk
05

Documentation and HS classification

Certificate of analysis, packing list, invoice and the HS line the shipment will actually be declared under, assembled as one file.

Container cranes at a northern European port of entry
06

EU port of entry

Rotterdam or Hamburg on the main routes. Clearance is where documentation is tested — and where the member-state legality gate begins.

Photographs are illustrative of the stages described, not of a specific consignment. Informational only — no medical claims, no consumer sales.

Plate — port of entry

Where the documentation is finally tested

Containers moving on the quay at a European port of entry
Clearance is the point at which every earlier stage is either evidenced or questioned. A consignment that cannot show its origin lot, its assay and its HS reasoning at the quay is a consignment that waits. Indicative, as of 2026.

Data column 1 · museum label: QC panel

Lab Assay Panel

Buyer-required quality control — not health data. Thresholds are indicative reference bands you should confirm against your own specification and lab report.

Buyer-required quality control · indicative, as of 2026
Parameter Method Typical reference threshold (indicative, as of 2026) Why EU buyers require it
Mitragynine HPLC ~1.0–2.0% Potency & authenticity spec
7-hydroxymitragynine HPLC <0.1% typical Batch-consistency marker
Lead (Pb) ICP-MS ≤3.0 ppm Heavy-metal safety limit
Arsenic (As) ICP-MS ≤1.5 ppm Heavy-metal safety limit
Cadmium (Cd) ICP-MS ≤1.0 ppm Heavy-metal safety limit
Mercury (Hg) ICP-MS ≤0.1 ppm Heavy-metal safety limit
Total plate count Micro (culture) ≤10⁴ CFU/g Microbial load control
Yeast & mould Micro (culture) ≤10³ CFU/g Microbial load control
E. coli Micro (culture) Absent / negative Pathogen screen
Salmonella Micro (culture) Absent in 25 g Pathogen screen
Moisture / loss-on-drying Gravimetric ≤10% Stability & shelf-life spec
Informational only — verify with the competent authority. Laboratory Testing Choosing Laboratories

Data column 2 · museum label: spec bands

Grade & Specification

Indicative spec bands for the three product forms, with the contract-term note that tolerances are written into supply contracts. All bands date-stamped indicative 2026.

Dried whole leaf

Mitragynine
~1.2–1.8%
Moisture
≤10%
Mesh / particle
Whole / cut leaf
Appearance
Green, low stem

Contract-term note: potency & foreign-matter tolerances set per lot.

Milled powder

Mitragynine
~1.0–1.6%
Moisture
≤10%
Mesh / particle
60–80 mesh
Appearance
Fine green powder

Contract-term note: mesh & colour band agreed on approved sample.

Standardized extract

Mitragynine
standardized band
Moisture
≤6%
Standardization
Declared assay %
Residual solvent
Reference limits apply

Contract-term note: standardization %, carrier & solvent references written into contract.

Sources: Defining Kratom Quality · West Kalimantan Origin & Grades.

Data column 3 · museum label: logistics

Route & Incoterm Board

Who bears what across the Incoterm ladder, the main Indonesia–Europe routes, and indicative transit bands. Confirm against a live quotation.

Incoterm ladder

EXW
Buyer bears everything from the Bali gate onward.
FOB
Seller delivers loaded on vessel at origin port.
CFR
Seller pays main sea freight; risk passes at loading.
CIF
CFR plus minimum marine insurance by seller.
DDP
Seller delivers cleared at destination — max seller duty.

Main routes & transit

Mode Origin Destination Transit (indicative)
Sea (FCL/LCL) Surabaya / Tj. Priok Rotterdam / Hamburg ~28–40 days
Air CGK Jakarta EU gateway ~3–7 days

HS-heading note: classification is declared on the PEB and confirmed at clearance — see Customs Clearance & HS Classification.

Sources: Shipping & Incoterms · Customs Clearance.

Data column 4 · museum label: legality landscape

EU Member-State Legality

Plain informational status labels per destination market. This is not legal advice.

Kratom is not authorised as a novel food EU-wide, and member-state rules differ. Informational only — verify current status with the competent authority before any transaction.

Sources: EU Novel Food & Member-State Legality · EU Trade-Compliance Checklist.

How the desk works

Honest, informational, verifiable

01

Assay first

Every consignment is framed around an accredited-lab COA — alkaloid, heavy-metal and microbial panels. QC data, never health data.

02

GMP-grade handling

Drying, milling and packing under documented controls, with a batch record that follows the goods to port.

03

Traceable origin

Leaf sourced from West Kalimantan smallholders with origin logged from the first station on the line.

We are a trade desk. Where we broker or coordinate on behalf of a producer, we say so plainly. No fabricated ratings, awards or client logos appear on this page — only date-stamped, indicative reference figures you should verify.

Five from the 100-question FAQ

Frequently asked

Do you make any medical or health claims about kratom?
No. This is an informational trade publication for B2B buyers. We publish export, quality-control and compliance information only — never medical, therapeutic or consumer-benefit claims.
Is kratom authorised as a novel food in the EU?
No — kratom is not authorised as a novel food EU-wide, and member-state rules differ. Treat every status label here as indicative and verify with the competent authority in your destination country.
What lab tests do EU buyers typically require?
A botanical panel: mitragynine and 7-hydroxymitragynine by HPLC, heavy metals (Pb, As, Cd, Hg) by ICP-MS, and microbial screens (total plate count, yeast & mould, E. coli, Salmonella), plus moisture. See the Laboratory Testing briefing.
Which Incoterms and routes are typical to Europe?
The ladder runs EXW → FOB → CFR → CIF → DDP. Sea from Surabaya or Tanjung Priok to Rotterdam/Hamburg is roughly 28–40 days indicative; air from CGK is roughly 3–7 days. Confirm on a live quote.
Are the figures on this page fixed prices or guarantees?
No. Every band is marked "indicative, as of 2026." No prices are invented. Figures are reference points for your compliance team to verify, not quotations or guarantees.

Read all 100 questions

Talk to the trade desk

Request an indicative consignment brief

Tell us the product form, destination market and order tier. Our BD desk replies with an informational, verify-with-authority brief — no medical claims, no invented pricing.

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WhatsApp +62 811-3941-4563

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[email protected]

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A paid desk review of your import project before you contract.

Compliance Consultation

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Contact page

Desk hours

Monday – Friday
09:00 – 18:00 WITA
Saturday
09:00 – 13:00 WITA
Sunday
Closed

Jalan Sunset Road
Kuta, Badung, Bali 80361, Indonesia
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Informational only — we do not provide medical, legal or investment advice.

Informational only — we do not provide medical, legal or investment advice.

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