Taiwan FDA registration 0cd144125692f991abe11baf6eb6541a
“Snowden Pencer” Gynecologic laparoscope and accessories (Non-Sterile)
TW: “史諾頓賓士” 婦產科用腹腔鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION·Registered Sep 06, 2016 – Sep 06, 2021ExpiredRegistration details
- Analysis ID
- 0cd144125692f991abe11baf6eb6541a
- License Form
- Ministry of Health Medical Device Import No. 016964
- Customs Code
- DHA09401696406
Company information
- Manufacturer
- CAREFUSION
- Manufacturer Country
- United States
- 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
- Sep 06, 2016
- Expiry Date
- Sep 06, 2021
About this record
Access comprehensive regulatory information for “Snowden Pencer” Gynecologic laparoscope and 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 0cd144125692f991abe11baf6eb6541a and manufactured by CAREFUSION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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