Taiwan FDA registration 27a5ae4cac2a0bf709f69541b15396e3
"Baihang" root canal (unsterilized)
TW: "百航" 根管銼(未滅菌)
Taiwan·Risk Class 1·FOSHAN BEHN MEDICAL INSTRUMENT CO., LTD.·Registered Mar 25, 2021 – Mar 25, 2026ExpiredRegistration details
- Analysis ID
- 27a5ae4cac2a0bf709f69541b15396e3
- Customs Code
- DHA09600447300
Company information
- Manufacturer
- FOSHAN BEHN MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HUANG YA BIOMEDICAL TECHNOLOGY LTD.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 25, 2021
- Expiry Date
- Mar 25, 2026
About this record
Access comprehensive regulatory information for "Baihang" root canal (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 27a5ae4cac2a0bf709f69541b15396e3 and manufactured by FOSHAN BEHN MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is HUANG YA BIOMEDICAL TECHNOLOGY LTD..
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