"IZI" Obstetric-Gynecologic General Manual Instrument (Non-Sterile)
- Analysis ID
- 0fe13e877e9367d5d226074fcd165a5d
- License Form
- Ministry of Health Medical Device Import No. 013714
- Customs Code
- DHA09401371407
- Manufacturer
- IZI MEDICAL PRODUCTS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Qiatai Enterprise Co., Ltd
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L4520 General manual instruments for obstetrics and gynecology
- Import Information
- Imported from abroad
- Registration Date
- Dec 23, 2013
- Expiry Date
- Dec 23, 2018
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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.