Taiwan FDA registration 060de6c88d56a5d937466f2638dbe46a
"Heger" eosin blue identification medium (unsterilized)
TW: “賀格”伊紅美藍鑑別培養基(未滅菌)
Registration details
- Analysis ID
- 060de6c88d56a5d937466f2638dbe46a
- Customs Code
- DHA04400920800
Company information
- Manufacturer
- HAGER & WERKEN GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- DENTWEI INDUSTRY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Identification Medium (C.2320)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2320 Differential culture media
- Import Information
- import
Dates and status
- Registration Date
- Sep 17, 2010
- Expiry Date
- Sep 17, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heger" eosin blue identification medium (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 060de6c88d56a5d937466f2638dbe46a and manufactured by HAGER & WERKEN GMBH & CO. KG. The authorized representative in Taiwan is DENTWEI INDUSTRY 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