Taiwan FDA registration 5263620ce33bb6a7a5090e0977d8c4d3
“Angiomed” Soft-Drain Nephrostomy Set
TW: “安吉美爾德”經皮腎造口引流管組
Taiwan·Risk Class 2·MD·ANGIOMED GMBH & CO.MEDIZINTECHNIK KG·Registered Aug 23, 2017 – Aug 23, 2022ExpiredRegistration details
- Analysis ID
- 5263620ce33bb6a7a5090e0977d8c4d3
- License Form
- Ministry of Health Medical Device Import No. 030132
- Customs Code
- DHA05603013201
Company information
- Manufacturer
- ANGIOMED GMBH & CO.MEDIZINTECHNIK KG
- Manufacturer Country
- Germany
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
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)
- H5130 Urinary catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 23, 2017
- Expiry Date
- Aug 23, 2022
About this record
Access comprehensive regulatory information for “Angiomed” Soft-Drain Nephrostomy Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5263620ce33bb6a7a5090e0977d8c4d3 and manufactured by ANGIOMED GMBH & CO.MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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