Taiwan FDA registration 266d3569acfa6581e42ee907238d66fa
Pe-Ha-Luron F 3.0%
TW: 愛玻美德人工玻璃體3.0%
Taiwan·Risk Class 3·MD·Albomed GmbH·Registered Mar 13, 2017 – Mar 13, 2027ActiveRegistration details
- Analysis ID
- 266d3569acfa6581e42ee907238d66fa
- License Form
- Ministry of Health Medical Device Import No. 029408
- Customs Code
- DHA05602940803
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 13, 2017
- Expiry Date
- Mar 13, 2027
About this record
Access comprehensive regulatory information for Pe-Ha-Luron F 3.0% in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 266d3569acfa6581e42ee907238d66fa and manufactured by Albomed GmbH. The authorized representative in Taiwan is INTELLIGENT-BIO CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices