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“Snowden Pencer” Gynecologic laparoscope and accessories (Non-Sterile) - Taiwan Registration 0cd144125692f991abe11baf6eb6541a

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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0cd144125692f991abe11baf6eb6541a
Registration Details
Taiwan FDA Registration: 0cd144125692f991abe11baf6eb6541a
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Device Details

“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)
Risk Class 1
MD

Registration Details

0cd144125692f991abe11baf6eb6541a

Ministry of Health Medical Device Import No. 016964

DHA09401696406

Company Information

United States

Product Details

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)".

l Devices for obstetrics and gynecology

L1720 Laparoscopy for obstetrics and gynecology and its accessories

Imported from abroad

Dates and Status

Sep 06, 2016

Sep 06, 2021