Taiwan FDA registration 38ab3dc2e650a0223f2e1644af24b506
Allium Biliary Stent(BIS) System
TW: 雅琉恩膽管支架組
Taiwan·Risk Class 2·MD·Allium Ltd.·Registered Dec 15, 2017 – Dec 15, 2027ActiveRegistration details
- Analysis ID
- 38ab3dc2e650a0223f2e1644af24b506
- License Form
- Ministry of Health Medical Device Import No. 030597
- Customs Code
- DHA05603059706
Company information
- Manufacturer
- Allium Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- HUILI MEDICAL EQUIPMENT LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5010 Bile ductal catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 15, 2017
- Expiry Date
- Dec 15, 2027
About this record
Access comprehensive regulatory information for Allium Biliary Stent(BIS) System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38ab3dc2e650a0223f2e1644af24b506 and manufactured by Allium Ltd.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.
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