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"Peters Surgery" Katifron surgical sutures - Taiwan Registration d2746c8d5a9d10e72f2ea36db52d10bf

Access comprehensive regulatory information for "Peters Surgery" Katifron surgical sutures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2746c8d5a9d10e72f2ea36db52d10bf and manufactured by PETERS SURGICAL. The authorized representative in Taiwan is ANSON HEALTH CARE INC..

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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d2746c8d5a9d10e72f2ea36db52d10bf
Registration Details
Taiwan FDA Registration: d2746c8d5a9d10e72f2ea36db52d10bf
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Device Details

"Peters Surgery" Katifron surgical sutures
TW: โ€œๅฝผๅพ—ๆ–ฏๅค–็ง‘โ€ๅก่’‚ๅผ—้พๅค–็ง‘็ธซๅˆ็ทš
Risk Class 2
Cancelled

Registration Details

d2746c8d5a9d10e72f2ea36db52d10bf

DHA00602041501

Company Information

France

Product Details

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

I General, Plastic Surgery and Dermatology

I.5000 Non-absorbable polyethylene terephthalate sewing wire

import

Dates and Status

Nov 18, 2009

Nov 18, 2014

May 28, 2018

Cancellation Information

Logged out

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