Taiwan FDA registration 1b66642a0e5e113727715d4822fec4c2
“Promedon” NAZCA Kit
TW: “博美登”納斯卡骨盆底修復套組
Taiwan·Risk Class 3·MD·Promedon S.A.·Registered Apr 21, 2015 – Apr 21, 2020CancelledRegistration details
- Analysis ID
- 1b66642a0e5e113727715d4822fec4c2
- License Form
- Ministry of Health Medical Device Import No. 027164
- Customs Code
- DHA05602716404
Company information
- Manufacturer
- Promedon S.A.
- Manufacturer Country
- Argentina
- Authorized Representative
- JIANHE BIO-MEDICAL LTD.
Product details
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L5980 Surgical mesh for transvaginal pelvic organ prolapse treatment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 21, 2015
- Expiry Date
- Apr 21, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Promedon” NAZCA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1b66642a0e5e113727715d4822fec4c2 and manufactured by Promedon S.A.. The authorized representative in Taiwan is JIANHE BIO-MEDICAL LTD..
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