Taiwan FDA registration ad98da5d541a8e1be2bed06d5d9d483b
Birlanc drip infusion sleeve
TW: 柏朗點滴輸液套
Taiwan·Risk Class 2·B.BRAUN MELSUNGEN AG;; DRAGON HEART MEDICAL DEVICES CO., LTD.·Registered Nov 24, 2008 – Nov 24, 2013CancelledRegistration details
- Analysis ID
- ad98da5d541a8e1be2bed06d5d9d483b
- Customs Code
- DHA04200018706
Company information
- Manufacturer Country
- Germany;;China
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5440 血管內輸液套
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Nov 24, 2008
- Expiry Date
- Nov 24, 2013
- Cancellation Date
- Apr 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Birlanc drip infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ad98da5d541a8e1be2bed06d5d9d483b and manufactured by B.BRAUN MELSUNGEN AG;; DRAGON HEART MEDICAL DEVICES CO., LTD.. The authorized representative in Taiwan is B. BRAUN TAIWAN 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