Taiwan FDA registration 5503108b592e81e58d9e2f6267d530ed
Cenefom Ophthalmic Sponge
TW: Cenefom眼科用泡棉
Taiwan·Risk Class 2·MD·CENEFOM CORP.·Registered Oct 18, 2018 – Oct 18, 2028ActiveRegistration details
- Analysis ID
- 5503108b592e81e58d9e2f6267d530ed
- License Form
- Ministry of Health Medical Device Manufacturing No. 006217
Company information
- Manufacturer
- CENEFOM CORP.
- 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 Ophthalmic devices
- Product Type (Level 2)
- M4790 Sponge for ophthalmic use
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 18, 2018
- Expiry Date
- Oct 18, 2028
About this record
Access comprehensive regulatory information for Cenefom Ophthalmic Sponge in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5503108b592e81e58d9e2f6267d530ed and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is CENEFOM CORP..
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