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"IZI" Obstetric-Gynecologic General Manual Instrument (Non-Sterile) - Taiwan Registration 0fe13e877e9367d5d226074fcd165a5d

Access comprehensive regulatory information for "IZI" Obstetric-Gynecologic General Manual Instrument (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 0fe13e877e9367d5d226074fcd165a5d and manufactured by IZI MEDICAL PRODUCTS, LLC. The authorized representative in Taiwan is Qiatai Enterprise Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IZI MEDICAL PRODUCTS, LLC, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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0fe13e877e9367d5d226074fcd165a5d
Registration Details
Taiwan FDA Registration: 0fe13e877e9367d5d226074fcd165a5d
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Device Details

"IZI" Obstetric-Gynecologic General Manual Instrument (Non-Sterile)
TW: "ๆ„›็ซ‹่‰พ"ๅฉฆ็”ข็ง‘็”จไธ€่ˆฌๆ‰‹ๅ‹•ๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

0fe13e877e9367d5d226074fcd165a5d

Ministry of Health Medical Device Import No. 013714

DHA09401371407

Company Information

United States

Product Details

l Devices for obstetrics and gynecology

L4520 General manual instruments for obstetrics and gynecology

Imported from abroad

Dates and Status

Dec 23, 2013

Dec 23, 2018

Jul 15, 2022

Cancellation Information

Logged out

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