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“Promedon” Splentis POP Tissue Anchoring System - Taiwan Registration 0c64894cb7cb06e143a2b5a98170d440

Access comprehensive regulatory information for “Promedon” Splentis POP Tissue Anchoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c64894cb7cb06e143a2b5a98170d440 and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee 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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0c64894cb7cb06e143a2b5a98170d440
Registration Details
Taiwan FDA Registration: 0c64894cb7cb06e143a2b5a98170d440
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Device Details

“Promedon” Splentis POP Tissue Anchoring System
TW: “博美敦”絲布藍脫垂修補系統
Risk Class 3
MD

Registration Details

0c64894cb7cb06e143a2b5a98170d440

Ministry of Health Medical Device Import No. 026790

DHA05602679001

Company Information

Argentina

Product Details

For details, it is Chinese approved copy of the imitation order

l Devices for obstetrics and gynecology

L5980 Surgical mesh for transvaginal pelvic organ prolapse treatment

Imported from abroad

Dates and Status

Nov 19, 2014

Nov 19, 2024