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"IZI" Obstetric-Gynecologic General Manual Instrument (Non-sterile) - Taiwan Registration bcfcd8657accbe44a8300192df6ad12e

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 bcfcd8657accbe44a8300192df6ad12e and manufactured by IZI MEDICAL PRODUCTS, LLC. The authorized representative in Taiwan is Cooperative L.F. Enterprise Co..

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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bcfcd8657accbe44a8300192df6ad12e
Registration Details
Taiwan FDA Registration: bcfcd8657accbe44a8300192df6ad12e
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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

Registration Details

bcfcd8657accbe44a8300192df6ad12e

Ministry of Health Medical Device Import No. 020310

DHA09402031000

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".

l Devices for obstetrics and gynecology

L4520 General manual instruments for obstetrics and gynecology

Imported from abroad

Dates and Status

Apr 12, 2019

Apr 12, 2024

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