Taiwan FDA registration 2af76d32d73dc4d337d8efdd9d5fc32e
“WAVE PEP”Dental Hand Instrument (Non-sterile)
TW: “偉平”牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·FRANK DENTAL GMBH·Registered Sep 09, 2021 – Sep 09, 2026ActiveRegistration details
- Analysis ID
- 2af76d32d73dc4d337d8efdd9d5fc32e
- License Form
- Ministry of Health Medical Device Import No. 022642
- Customs Code
- DHA09402264209
Company information
- Manufacturer
- FRANK DENTAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WAVE PEP TRADE CO., 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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 09, 2021
- Expiry Date
- Sep 09, 2026
About this record
Access comprehensive regulatory information for “WAVE PEP”Dental Hand Instrument (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 2af76d32d73dc4d337d8efdd9d5fc32e and manufactured by FRANK DENTAL GMBH. The authorized representative in Taiwan is WAVE PEP TRADE CO., LTD..
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