Taiwan FDA registration 67bdbba5bfaea9089d26faa7ea6b0a0c
“V. Mueller” Gynecologic laparoscope and accessories (Non-Sterile)
TW: “米穆勒” 婦產科用腹腔鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION·Registered Sep 12, 2017 – Sep 12, 2022ExpiredRegistration details
- Analysis ID
- 67bdbba5bfaea9089d26faa7ea6b0a0c
- License Form
- Ministry of Health Medical Device Import No. 018306
- Customs Code
- DHA09401830604
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 12, 2017
- Expiry Date
- Sep 12, 2022
About this record
Access comprehensive regulatory information for “V. Mueller” 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 67bdbba5bfaea9089d26faa7ea6b0a0c and manufactured by CAREFUSION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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