Taiwan FDA registration 75bc8a1bac341e5390df6179d29bee75
"Telmau" vacuum blood collection vessels
TW: "泰爾茂" 真空採血管
Taiwan·Risk Class 2·TERUMO CORPORATION;; KOFU FACTORY OF TERUMO CORPORATION·Registered Mar 14, 2006 – Mar 14, 2011CancelledRegistration details
- Analysis ID
- 75bc8a1bac341e5390df6179d29bee75
- Customs Code
- DHA00601613700
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- Taipei Branch of Nissho Termo Co., Ltd
Product details
- Intended Use
- A test tube for blood collection for serological examination.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1675 Blood collection equipment
- Import Information
- import
Dates and status
- Registration Date
- Mar 14, 2006
- Expiry Date
- Mar 14, 2011
- Cancellation Date
- Apr 03, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Telmau" vacuum blood collection vessels in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75bc8a1bac341e5390df6179d29bee75 and manufactured by TERUMO CORPORATION;; KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is Taipei Branch of Nissho Termo 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