Taiwan FDA registration 2fba3e4c8fd7a8bdef7aa692ab8c87c1
"Merck" Differential culture medium (Non-Sterile)
TW: "默克" 鑑別培養基 (未滅菌)
Taiwan·Risk Class 1·MD·MERCK KGAA·Registered May 06, 2020 – May 06, 2025ExpiredRegistration details
- Analysis ID
- 2fba3e4c8fd7a8bdef7aa692ab8c87c1
- License Form
- Ministry of Health Medical Device Import No. 021519
- Customs Code
- DHA09402151905
Company information
- Manufacturer
- MERCK KGAA
- Manufacturer Country
- Germany
- Authorized Representative
- MERCK 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 devices
- Product Type (Level 2)
- C2320 Differential medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 06, 2020
- Expiry Date
- May 06, 2025
About this record
Access comprehensive regulatory information for "Merck" Differential culture medium (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2fba3e4c8fd7a8bdef7aa692ab8c87c1 and manufactured by MERCK KGAA. The authorized representative in Taiwan is MERCK LTD..
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