Sri Trang Gloves
Einweghandschuhe aus Latex und Nitril für medizinische und industrielle Zwecke.
Sri Trang Gloves stellt Untersuchungshandschuhe aus Latex und Nitril an Produktionsstandorten in ganz Thailand her. Das Unternehmen beliefert weltweit Kunden aus den Bereichen Medizin, Lebensmittel, Labor und Industriesicherheit.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Bangkok, Thailand
- Founded
- 1989
- Website
- sritranggloves.com
- Categories
- Medizin- & Gesundheitsbedarf, Sicherheits- & Schutzausrüstung, Gummi & Verbundwerkstoffe
- Markets
- Thailand, Vereinigte Staaten, Deutschland, Japan
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-12 Domain registry record
- registry-activity (green), checked 2026-08-15 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- fda-registered (green), checked 2026-08-12 FDA
- financials-published (green), effective since 2025-12-31 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- registry-id-verified (green), checked 2026-08-20 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Protective equipment (helmets, gloves, eyewear) sold in the EU falls under the PPE Regulation (EU) 2016/425 and needs CE marking. European Commission (PPE)