Taiwan FDA registration 50c1802f5703821f6e5ea0896db05168
"Merck" Enriched culture medium (Non-Sterile)
TW: "默克" 強化培養基 (未滅菌)
Taiwan·Risk Class 1·MD·MERCK KGAA·Registered May 06, 2020 – May 06, 2025ExpiredRegistration details
- Analysis ID
- 50c1802f5703821f6e5ea0896db05168
- License Form
- Ministry of Health Medical Device Import No. 021520
- Customs Code
- DHA09402152003
Company information
- Manufacturer
- MERCK KGAA
- Manufacturer Country
- Germany
- Authorized Representative
- MERCK LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Intensive Medium (C.2330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2330 fortified 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" Enriched 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 50c1802f5703821f6e5ea0896db05168 and manufactured by MERCK KGAA. The authorized representative in Taiwan is MERCK LTD..
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