Taiwan FDA registration 22b8859188e294f65087176f248aaf85
"BRAINLAB" Surgical Instruments (Non-Sterile)
TW: "百靈列" 手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·BRAINLAB AG·Registered Feb 17, 2017 – Feb 17, 2027ActiveRegistration details
- Analysis ID
- 22b8859188e294f65087176f248aaf85
- License Form
- Ministry of Health Medical Device Import No. 017502
- Customs Code
- DHA09401750202
Company information
- Manufacturer
- BRAINLAB AG
- Manufacturer Country
- Germany
- Authorized Representative
- BARRY TEC ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2017
- Expiry Date
- Feb 17, 2027
About this record
Access comprehensive regulatory information for "BRAINLAB" Surgical Instruments (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 22b8859188e294f65087176f248aaf85 and manufactured by BRAINLAB AG. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..
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