Sri Trang Gloves
의료 및 산업용 일회용 라텍스 및 니트릴 장갑.
Sri Trang 장갑은 태국 전역의 생산 현장에서 라텍스 및 니트릴 검사 장갑을 제조합니다. 이 회사는 전 세계 의료, 식품, 실험실 및 산업 안전 고객에게 제품을 공급합니다.
- Type
- Manufacturer
- Location
- Bangkok, Thailand
- Founded
- 1989
- Website
- sritranggloves.com
- Categories
- 의료 및 건강 관리 용품, 안전 및 보호 장비, 고무 및 복합제품
- Markets
- 태국, 미국, 독일, 일본
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), checked 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
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
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)
- Chemical substances imported into the EU above 1 tonne/year must be REACH-registered. ECHA (REACH)