Taiwan FDA registration a6776c95708805e30a6371ed13a038b5
"Interlock" Manual surgical instrument for general use (Non-Sterile)
TW: "安特樂可" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·INTERLOCK MEDIZINTECHNIK GMBH·Registered Jun 05, 2019 – Jun 05, 2024ExpiredRegistration details
- Analysis ID
- a6776c95708805e30a6371ed13a038b5
- License Form
- Ministry of Health Medical Device Import No. 020524
- Customs Code
- DHA09402052406
Company information
- Manufacturer
- INTERLOCK MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- RECHI 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
- Jun 05, 2019
- Expiry Date
- Jun 05, 2024
About this record
Access comprehensive regulatory information for "Interlock" 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 a6776c95708805e30a6371ed13a038b5 and manufactured by INTERLOCK MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is RECHI CO., LTD..
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