Taiwan FDA registration 620aaf94e867ae95232bf8f7ede2b052
"New Dura" dural (spine) membrane patch
TW: “新杜拉”硬腦(脊)膜補片
Registration details
- Analysis ID
- 620aaf94e867ae95232bf8f7ede2b052
- Customs Code
- DHA09200135907
Company information
- Manufacturer Country
- Germany;;China
- Authorized Representative
- PAONAN BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5910 Dural replacement
- Import Information
- Chinese goods;; Input;; Contract manufacturing
Dates and status
- Registration Date
- May 10, 2022
- Expiry Date
- May 10, 2027
About this record
Access comprehensive regulatory information for "New Dura" dural (spine) membrane patch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 620aaf94e867ae95232bf8f7ede2b052 and manufactured by Medprin Biotech GmbH;; Medprin Regenerative Medical Technologies Co., Ltd.. The authorized representative in Taiwan is PAONAN 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