Taiwan FDA registration dd6c3e1ab95840b79996106228a33994
"Gebrueder Zepf" Manual surgical instrument for general use (Non-Sterile)
TW: "基博德塞夫" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·GEBRUEDER ZEPF MEDIZINTECHNIK GMBH & CO. KG·Registered Dec 05, 2013 – Dec 05, 2023ExpiredRegistration details
- Analysis ID
- dd6c3e1ab95840b79996106228a33994
- License Form
- Ministry of Health Medical Device Import No. 013658
- Customs Code
- DHA09401365800
Company information
- Manufacturer
- GEBRUEDER ZEPF MEDIZINTECHNIK GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- PLOVER MEDICAL INSTRUMENTS, INC.
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
- Dec 05, 2013
- Expiry Date
- Dec 05, 2023
About this record
Access comprehensive regulatory information for "Gebrueder Zepf" Manual surgical instrument for general use (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 dd6c3e1ab95840b79996106228a33994 and manufactured by GEBRUEDER ZEPF MEDIZINTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, INC..
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