Taiwan FDA registration 954cc92c4bf1b81b6616d29b11f1c7cf
"Ulrich" Pneumatic Tourniquet (Non-Sterile)
TW: "歐利奇" 充氣式止血帶 (未滅菌)
Registration details
- Analysis ID
- 954cc92c4bf1b81b6616d29b11f1c7cf
- License Form
- Ministry of Health Medical Device Import No. 020533
- Customs Code
- DHA09402053307
Company information
- Manufacturer
- ULRICH GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- SINCERE BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I5910 Inflatable tourniquet
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 10, 2019
- Expiry Date
- Jun 10, 2024
About this record
Access comprehensive regulatory information for "Ulrich" Pneumatic Tourniquet (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 954cc92c4bf1b81b6616d29b11f1c7cf and manufactured by ULRICH GMBH & CO. KG. The authorized representative in Taiwan is SINCERE BIOTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices