Taiwan FDA registration 4ee252e017641d957b7d156b21e360bb
"Snowden Pencer/ V. Mueller" Manual surgical instrument for general use (Non-Sterile)
TW: "史諾頓賓士/米穆勒" 一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION GERMANY 318 GMBH·Registered Jun 20, 2018 – Jun 20, 2023ExpiredRegistration details
- Analysis ID
- 4ee252e017641d957b7d156b21e360bb
- License Form
- Ministry of Health Medical Device Import No. 019200
- Customs Code
- DHA09401920006
Company information
- Manufacturer
- CAREFUSION GERMANY 318 GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- DOUBLE-SUCCESS 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 20, 2018
- Expiry Date
- Jun 20, 2023
About this record
Access comprehensive regulatory information for "Snowden Pencer/ V. Mueller" 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 4ee252e017641d957b7d156b21e360bb and manufactured by CAREFUSION GERMANY 318 GMBH. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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