Taiwan FDA registration 91a9f68f4a3f590f4746b720e65d9e95
Pe-Ha-Luron F 1.8%
TW: 愛玻美德人工玻璃體1.8%
Taiwan·Risk Class 3·MD·Albomed GmbH·Registered Mar 17, 2017 – Mar 17, 2027ActiveRegistration details
- Analysis ID
- 91a9f68f4a3f590f4746b720e65d9e95
- License Form
- Ministry of Health Medical Device Import No. 029412
- Customs Code
- DHA05602941207
Company information
- Manufacturer
- Albomed GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- INTELLIGENT-BIO CO., LTD.
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)
- M4275 Liquid for intraocular filling
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 17, 2017
- Expiry Date
- Mar 17, 2027
About this record
Access comprehensive regulatory information for Pe-Ha-Luron F 1.8% in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 91a9f68f4a3f590f4746b720e65d9e95 and manufactured by Albomed GmbH. The authorized representative in Taiwan is INTELLIGENT-BIO CO., LTD..
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