Taiwan FDA registration 7093319e3053bac66c844e6f864e2d15
“Merck” Anaerobiosis Gas-generating Device System (Non-sterile)
TW: “默克”產氣器材組 (未滅菌)
Taiwan·Risk Class 1·MD·MERCK KGAA·Registered Jan 22, 2014 – Jan 22, 2024ExpiredRegistration details
- Analysis ID
- 7093319e3053bac66c844e6f864e2d15
- License Form
- Ministry of Health Medical Device Import No. 013805
- Customs Code
- DHA09401380500
Company information
- Manufacturer
- MERCK KGAA
- Manufacturer Country
- Germany
- Authorized Representative
- MERCK LTD.
Product details
- Intended Use
- Limited to the first level identification scope of medical equipment management measures "Gas Production Equipment (C.2580)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2580 Gas Production Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 22, 2014
- Expiry Date
- Jan 22, 2024
About this record
Access comprehensive regulatory information for “Merck” Anaerobiosis Gas-generating Device System (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 7093319e3053bac66c844e6f864e2d15 and manufactured by MERCK KGAA. The authorized representative in Taiwan is MERCK LTD..
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