Evidence organized for serious buyers.
Our quality approach begins with the written product requirement and continues through material review, approved samples, production controls, lot inspection, traceability, packaging approval, and release documentation. The available SGS reports show selected testing on identified glove samples. They support due diligence, but they do not establish universal approval for every TEC CARE product, production lot, claim, or country.
Independent testing and accreditation context.
These marks are displayed as documentary context only. They must be interpreted with the issuing report, laboratory scope, dates, tested sample, and applicable rules.
Independent testing
The displayed documents were issued by SGS-CSTC for the submitted samples and selected tests identified in each report.
Laboratory accreditation mark
CNAS marks shown on the reports relate to the issuing laboratory and accredited scope—not blanket product approval.
International recognition arrangement
The ILAC-MRA mark shown supports recognition of accredited laboratory results within the applicable arrangement and scope.
China inspection-body qualification mark
The CMA mark appears on the Chinese-language SGS report. Its exact legal meaning and scope must be read with that report.
Available SGS glove test reports.
The documents are kept inside PDF files rather than displayed on the webpage. Open a card to review the actual available first-page file and its visible scope.
Latex glove test report
Disposable latex gloves
- Reference
- SL221092271747501TX
- Standard / scope
- EN ISO 21420 clauses shown
- Issue date shown
- June 11, 2021
Vinyl glove test report
Disposable vinyl gloves
- Reference
- SL221092271748001TX
- Standard / scope
- EN ISO 21420 clauses shown
- Issue date shown
- June 11, 2021
Nitrile glove test report
Disposable nitrile gloves
- Reference
- SL221092271748201TX
- Standard / scope
- EN ISO 21420 clauses shown
- Issue date shown
- June 11, 2021
Chinese-language SGS test report
Product and scope shown in document
- Reference
- SHAHG2111392701
- Standard / scope
- Report SHAHG2111392701
- Issue date shown
- June 10, 2021
Every market checks the exact product—not the company name alone.
Government agencies and conformity routes are shown as verification pathways, not as claimed approvals. Before sale, the buyer and responsible economic operators must match the exact product, intended use, classification, manufacturer, authorization, labels, and current records.
United States · FDA
Medical examination gloves generally require the exact device’s FDA 510(k) clearance and compliant establishment, listing, labeling, and importer records. No HENYO/TEC CARE FDA clearance is claimed here without the matching official record.
European Union · CE / MDR
A CE mark for a medical device follows the applicable MDR conformity route and technical documentation. The SGS reports shown here are not, by themselves, CE certificates or declarations of conformity.
Great Britain · MHRA
Medical devices placed on the Great Britain market must follow the applicable UK registration, conformity-marking, responsible-person, and labeling route. Confirm the exact product record before supply.
Canada · Health Canada
Class and activity determine Medical Device Licence and establishment-licence responsibilities. Confirm the exact device and current licence pathway before import or sale.
China · NMPA / market classification
Classification, product registration or filing, production, labeling, and standards must be reviewed for the exact intended use in China. An export test report is not a substitute for a required domestic authorization.
Confirm the document against the exact supply before purchase.
Validity, scope, referenced standards, product type, manufacturer, model, intended use, and destination-market acceptance can differ. Request the current full document set for the exact product being quoted and have qualified personnel review it before approval, import, distribution, or use.