Taiwan FDA registration e36e2b6c769ac551823b6caa892e0fdd
"Ulikang" Glass Expo(Not Wiped Out)
TW: "佑立康" 玻露肛門護膜(未滅菌)
Registration details
- Analysis ID
- e36e2b6c769ac551823b6caa892e0fdd
- Customs Code
- DHA09402337402
Company information
- Manufacturer
- BIOFACTOR SP. ZO. O.
- Manufacturer Country
- Poland
- Authorized Representative
- UNIMED PHARMACEUTICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5090 Liquid bandages
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 22, 2024
- Expiry Date
- Jan 22, 2029
About this record
Access comprehensive regulatory information for "Ulikang" Glass Expo(Not Wiped Out) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e36e2b6c769ac551823b6caa892e0fdd and manufactured by BIOFACTOR SP. ZO. O.. The authorized representative in Taiwan is UNIMED PHARMACEUTICAL ENTERPRISE CO., LTD..
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