Sri Trang Gloves
医療用および産業用のラテックスおよびニトリル使い捨て手袋。
Sri Trang Gloves は、タイ全土の生産拠点でラテックスとニトリルの検査用手袋を製造しています。同社は、世界中の医療、食品、実験室、産業安全の顧客に製品を提供しています。
- Type
- Manufacturer
- Location
- Bangkok, Thailand
- Founded
- 1989
- Website
- sritranggloves.com
- Categories
- 医療およびヘルスケア用品, 安全および保護装置, ゴムおよび複合製品
- Markets
- タイ, アメリカ合衆国, ドイツ, 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)