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Pe-Ha-Luron F 1.8% - Taiwan Registration 91a9f68f4a3f590f4746b720e65d9e95

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..

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.

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91a9f68f4a3f590f4746b720e65d9e95
Registration Details
Taiwan FDA Registration: 91a9f68f4a3f590f4746b720e65d9e95
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Device Details

Pe-Ha-Luron F 1.8%
TW: ๆ„›็Žป็พŽๅพทไบบๅทฅ็Žป็’ƒ้ซ”1.8%
Risk Class 3
MD

Registration Details

91a9f68f4a3f590f4746b720e65d9e95

Ministry of Health Medical Device Import No. 029412

DHA05602941207

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M4275 Liquid for intraocular filling

Imported from abroad

Dates and Status

Mar 17, 2017

Mar 17, 2027