Taiwan FDA registration 3100c2fb26811295bd67a6956bf57329
"Snowden Pencer/ V. Mueller" Gynecologic laparoscope accessories (Non-Sterile)
TW: "史諾頓賓士/米穆勒"婦產科用腹腔鏡附件(未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION GERMANY 318 GMBH·Registered Jun 20, 2018 – Jun 20, 2023ExpiredRegistration details
- Analysis ID
- 3100c2fb26811295bd67a6956bf57329
- License Form
- Ministry of Health Medical Device Import No. 019201
- Customs Code
- DHA09401920108
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 "Laparoscopy and Its Accessories for Obstetrics and Gynecology (L.1720)".
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L1720 Laparoscopy for obstetrics and gynecology and its accessories
- 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" Gynecologic laparoscope accessories (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 3100c2fb26811295bd67a6956bf57329 and manufactured by CAREFUSION GERMANY 318 GMBH. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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