Taiwan FDA registration 7384d954420a19d58f7187c2a8db97d9
"Aiwei Medicine" Aiwei Modified Guide Tube
TW: “艾微醫學”艾微改導引導管
Taiwan·Risk Class 2·ALVIMEDICA TİBBİ Urunler SAN. AND EXTERNAL. T.C. Inc.·Registered Jul 08, 2013 – Jul 08, 2018CancelledRegistration details
- Analysis ID
- 7384d954420a19d58f7187c2a8db97d9
- Customs Code
- DHA00602520209
Company information
- Manufacturer Country
- Türkiye
- Authorized Representative
- JENS MEDICAL CONSULTING LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Jul 08, 2013
- Expiry Date
- Jul 08, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Aiwei Medicine" Aiwei Modified Guide Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7384d954420a19d58f7187c2a8db97d9 and manufactured by ALVIMEDICA TİBBİ Urunler SAN. AND EXTERNAL. T.C. Inc.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..
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