"IZI" Rectal Dilator (Non-Sterile)
Taiwan·Risk Class 1·MD·IZI MEDICAL PRODUCTS, LLC·Registered Dec 23, 2013 – Dec 23, 2018Cancelled- Analysis ID
- c58d8e0fa00bd7c23b44e7ddcf4a1674
- License Form
- Ministry of Health Medical Device Import No. 013713
- Customs Code
- DHA09401371305
- Manufacturer
- IZI MEDICAL PRODUCTS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Qiatai Enterprise Co., Ltd
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5450 Rectal dilators
- 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
Top companies providing products similar to ""IZI" Rectal Dilator (Non-Sterile)"
Recently registered similar products
Access comprehensive regulatory information for "IZI" Rectal Dilator (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 c58d8e0fa00bd7c23b44e7ddcf4a1674 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.