CERTIFICATIONS & COMPLIANCE
Compliance information must be read against the responsible entity, product or model, target market, document type, scope and current status.
Management-system certificates for Shaoxing Geeko Technology Co., Ltd.: ISO 9001:2015, Certificate No. 38125Q0229R0S; ISO 13485:2016, Certificate No. 381250175R0S; ISO 14001:2015, Certificate No. 38125E0107R0S; and ISO 45001:2018, Certificate No. 38125S0090R0S. The G61 CE/EMC, FCC and RoHS files are declarations of conformity, not management-system certificates.
G61 REACH Test Report No. ATJC25082780002600RH records testing from 2025-08-27 to 2025-08-30 and a result of ‘Meet requirement’ against the cited REACH SVHC requirement. The G61 EMC Declaration cites Reference Report No. ATJC25082780002600E, but a separate EMC Test Report file is not present in the current public asset set.
FY2026 FDA Establishment Registration Evidence for Shaoxing Geeko Technology Co., Ltd.; Owner / Operator No. 10096210; issued 2026-07-24 and expiring 2026-12-31. Establishment registration and listing are not FDA approval, certification or endorsement.
FDA Device Listing D604752; Product Code JEQ; Device Name: TOOTHBRUSH, POWERED. Proprietary names identify electric toothbrush models G51, G61, G71, G81 and G91. This listing does not represent FDA approval, certification or endorsement.
G61 only for the CE/EMC Declaration, FCC Supplier’s Declaration of Conformity, RoHS Declaration of Conformity and REACH Test Report. FDA registration / listing evidence identifies G51, G61, G71, G81 and G91. The ISO certificates cover management-system scope and are not model-specific product approvals.
EU evidence: G61 CE/EMC Declaration, RoHS Declaration and REACH Test Report. U.S. evidence: G61 FCC Supplier’s Declaration of Conformity plus FDA establishment registration / device listing for the listed models. ISO management-system certificates are company-scope evidence rather than market-specific product approvals; the ISO 13485 scope is marked export only.
ISO 9001, ISO 14001 and ISO 45001 scope: production and sales of electric toothbrushes. ISO 13485 scope: production and sales of electric toothbrushes (export only). Product evidence is limited to each source file: G61 for EMC Directive 2014/30/EU, FCC Part 15 Subpart B, RoHS and REACH; FDA evidence is limited to the five listed electric-toothbrush models.
ISO certificate numbers: 38125Q0229R0S, 381250175R0S, 38125E0107R0S and 38125S0090R0S. G61 document / reference numbers: EMC ATJC25082780002600E; FCC ATJC25082780002600F; RoHS ATJC25082780002600R; REACH ATJC25082780002600RH. FDA evidence: Owner / Operator No. 10096210 and Device Listing D604752, Product Code JEQ.
ISO 9001 and ISO 13485: issued 2025-06-13, valid through 2028-06-12. ISO 14001 and ISO 45001: issued 2025-06-18, valid through 2028-06-17. FDA FY2026 evidence: issued 2026-07-24, expires 2026-12-31. G61 EMC, FCC and RoHS declarations are dated 2025-08-30 with no expiry shown; the REACH report covers testing through 2025-08-30 and shows ‘Meet requirement’, with no expiry shown.
Use ‘View Document’ for each certificate, declaration and test report. Use ‘View Registration / Listing Evidence’ for the FDA asset. Verification references printed in the source documents remain the source of record; this local mapping adds no new external verification URL.
01
Start with the intended market, identify the exact product or model, then confirm the applicable certificate, test report, registration, listing or supporting document.
02
The framework covers market and product compliance, environmental and material compliance, U.S. FDA documentation and other supporting records only where formal evidence is available.
Available evidence is matched to the relevant product, model and intended market.
RoHS and REACH-related records are reviewed against their document scope and applicable product.
Establishment Registration, Device Listing and applicable model evidence are distinct records and do not constitute FDA approval.
Additional records are presented only when their source, scope and current status can be supported.
03
Document cards show only evidence-supported fields. Missing numbers, validity details or applicability are not inferred.
Available certificates or reports require document-level confirmation of holder, product or model, market, number, scope and validity.
The current record supports Shaoxing Geeko Technology Co., Ltd. establishment registration and device listing evidence for listed models G51, G61, G71, G81 and G91. R100-Z is not included.
04
A certificate, test report, registration and listing are different evidence objects. Each must be described according to what the underlying document actually establishes.
05
Requirements vary by target market and cannot be generalized without confirming the applicable product, function, configuration and evidence.
06
Applicable requirements may vary according to model, configuration, function and target market. Confirm these inputs before relying on a document for a project.
07
Manufacturing, OEM and ODM discussions can route into model- and market-specific compliance review.
Not necessarily. Applicability must be checked by model, configuration, function, target market and document scope.
No. A test report records testing and results within its scope; a certificate represents a different evidence type and must be read on its own terms.
No. Establishment Registration and Device Listing are not FDA approval, certification or endorsement.
Yes. Product, function or configuration changes may require renewed applicability review.
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