Sri Trang Gloves
用于医疗和工业用途的乳胶和丁腈一次性手套。
Sri Trang Gloves 在泰国各地的生产基地生产乳胶和丁腈检查手套。该公司为全球医疗、食品、实验室和工业安全客户提供服务。
- Type
- Manufacturer
- Location
- Bangkok, Thailand
- Founded
- 1989
- Website
- sritranggloves.com
- Categories
- 医疗保健用品, 安全及防护设备, 橡胶及复合材料产品
- Markets
- 泰国, 美国, 德国, 日本
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)