Taiwan FDA registration 10a0561639e315b2f8c0f530003a143b
"Interlock" instrument case (Non-Sterile)
TW: "英特拉克" 器械盒 (未滅菌)
Taiwan·Risk Class 1·MD·INTERLOCK MEDIZINTECKNIK GMBH·Registered Dec 10, 2018 – Dec 10, 2023ExpiredRegistration details
- Analysis ID
- 10a0561639e315b2f8c0f530003a143b
- License Form
- Ministry of Health Medical Device Import No. 019900
- Customs Code
- DHA09401990008
Company information
- Manufacturer
- INTERLOCK MEDIZINTECKNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- KINDMED CORPORATION
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 10, 2018
- Expiry Date
- Dec 10, 2023
About this record
Access comprehensive regulatory information for "Interlock" instrument case (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 10a0561639e315b2f8c0f530003a143b and manufactured by INTERLOCK MEDIZINTECKNIK GMBH. The authorized representative in Taiwan is KINDMED CORPORATION.
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