Taiwan FDA registration 68e38316ce5290dfa817206d323d9cbe
Cerefom ophthalmic foam
TW: Cenefom眼科用泡棉
Taiwan·Risk Class 2·INNOVATIVE MEDICAL MANUFACTURING COMPANY·Registered Apr 21, 2014 – Apr 21, 2024ExpiredRegistration details
- Analysis ID
- 68e38316ce5290dfa817206d323d9cbe
Company information
- Manufacturer
- INNOVATIVE MEDICAL MANUFACTURING COMPANY
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CENEFOM CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4790 Sponge for ophthalmic use
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 21, 2014
- Expiry Date
- Apr 21, 2024
- Cancellation Date
- Dec 29, 2022
About this record
Access comprehensive regulatory information for Cerefom ophthalmic foam in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68e38316ce5290dfa817206d323d9cbe and manufactured by INNOVATIVE MEDICAL MANUFACTURING COMPANY. The authorized representative in Taiwan is CENEFOM CORP..
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