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“Promedon” NAZCA Kit - Taiwan Registration 1b66642a0e5e113727715d4822fec4c2

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..

This page provides complete technical specifications, regulatory compliance details. 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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1b66642a0e5e113727715d4822fec4c2
Registration Details
Taiwan FDA Registration: 1b66642a0e5e113727715d4822fec4c2
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Device Details

“Promedon” NAZCA Kit
TW: “博美登”納斯卡骨盆底修復套組
Risk Class 3
MD
Cancelled

Registration Details

1b66642a0e5e113727715d4822fec4c2

Ministry of Health Medical Device Import No. 027164

DHA05602716404

Company Information

Argentina

Product Details

l Devices for obstetrics and gynecology

L5980 Surgical mesh for transvaginal pelvic organ prolapse treatment

Imported from abroad

Dates and Status

Apr 21, 2015

Apr 21, 2020

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者