Taiwan FDA registration 029872b13e810fd60c69fc91e68f627e
"Martin" manual instruments for general surgery (unsterilized)
TW: “馬汀”一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·GEBRÜDER MARTIN GMBH & CO. KG·Registered Jul 26, 2012 – Jul 26, 2017CancelledRegistration details
- Analysis ID
- 029872b13e810fd60c69fc91e68f627e
- Customs Code
- DHA04401198203
Company information
- Manufacturer
- GEBRÜDER MARTIN GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- P & H 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, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Jul 26, 2012
- Expiry Date
- Jul 26, 2017
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Martin" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 029872b13e810fd60c69fc91e68f627e and manufactured by GEBRÜDER MARTIN GMBH & CO. KG. The authorized representative in Taiwan is P & H BIOTECH CORP..
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