Taiwan FDA registration da1cbd2eea3e51b31f7930e2162dfe3b
"Gumei-Taiwan" Hand Instruments for Root Canal Dentistry (Sterilized/Unsterilized)
TW: “固美-台灣” 根管牙科手用器械 (滅菌/未滅菌)
Registration details
- Analysis ID
- da1cbd2eea3e51b31f7930e2162dfe3b
- Customs Code
- DHA09402126207
Company information
- Manufacturer
- GEBR. BRASSELER GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- UNITED MEDICAL SPECIALTIES CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Feb 13, 2020
- Expiry Date
- Feb 13, 2030
About this record
Access comprehensive regulatory information for "Gumei-Taiwan" Hand Instruments for Root Canal Dentistry (Sterilized/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da1cbd2eea3e51b31f7930e2162dfe3b and manufactured by GEBR. BRASSELER GMBH & CO. KG. The authorized representative in Taiwan is UNITED MEDICAL SPECIALTIES CORPORATION.
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