Taiwan FDA registration daa5ad0767e21374a1cf49277a8c777d
“Origen” Cryobag
TW: “奧尼根”冷凍保存袋
Taiwan·Risk Class 2·MD·Origen Biomedical Inc.·Registered Aug 02, 2018 – Aug 02, 2023ExpiredRegistration details
- Analysis ID
- daa5ad0767e21374a1cf49277a8c777d
- License Form
- Ministry of Health Medical Device Import No. 031381
- Customs Code
- DHA05603138101
Company information
- Manufacturer
- Origen Biomedical Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK 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)
- J9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 02, 2018
- Expiry Date
- Aug 02, 2023
About this record
Access comprehensive regulatory information for “Origen” Cryobag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number daa5ad0767e21374a1cf49277a8c777d and manufactured by Origen Biomedical Inc.. The authorized representative in Taiwan is Y.H. BIOTEK 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