Taiwan FDA registration c229b9f3569f2c6f083b7e87c86c9070
"BroadMaster" Lancing Devices (Non-Sterile)
TW: "博通生技"採血筆(未滅菌)
Taiwan·Risk Class 1·MD·GENTEEL LLC·Registered Jul 13, 2020 – Jul 13, 2025ExpiredRegistration details
- Analysis ID
- c229b9f3569f2c6f083b7e87c86c9070
- License Form
- Ministry of Health Medical Device Import No. 021733
- Customs Code
- DHA09402173307
Company information
- Manufacturer
- GENTEEL LLC
- Manufacturer Country
- United States
- Authorized Representative
- BROADMASTER BIOTECH. CORP.
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
- Jul 13, 2020
- Expiry Date
- Jul 13, 2025
About this record
Access comprehensive regulatory information for "BroadMaster" Lancing Devices (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 c229b9f3569f2c6f083b7e87c86c9070 and manufactured by GENTEEL LLC. The authorized representative in Taiwan is BROADMASTER BIOTECH. CORP..
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