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"Vidalik" titanium vascular clamp - Taiwan Registration d24254289e3d033898346063776eea9f

Access comprehensive regulatory information for "Vidalik" titanium vascular clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d24254289e3d033898346063776eea9f and manufactured by Peters Surgical. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PETERS SURGICAL, and 1 recent registrations in the same category. 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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d24254289e3d033898346063776eea9f
Registration Details
Taiwan FDA Registration: d24254289e3d033898346063776eea9f
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Device Details

"Vidalik" titanium vascular clamp
TW: โ€œ็ถญ้”ๅŠ›ๅ…‹โ€้ˆฆ้‡‘ๅฑฌ่ก€็ฎกๅคพ
Risk Class 2

Registration Details

d24254289e3d033898346063776eea9f

DHA00602327207

Company Information

France

Product Details

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

E Cardiovascular Medicine Science

E.4450 Vascular clips

import

Dates and Status

Mar 06, 2012

Mar 06, 2027

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