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"Payon" combined laparoscopic instrument - Taiwan Registration e272c3b521c771e819a77d48cbe3c054

Access comprehensive regulatory information for "Payon" combined laparoscopic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e272c3b521c771e819a77d48cbe3c054 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments 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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e272c3b521c771e819a77d48cbe3c054
Registration Details
Taiwan FDA Registration: e272c3b521c771e819a77d48cbe3c054
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Device Details

"Payon" combined laparoscopic instrument
TW: "ๅธ•ๆฐธ"็ต„ๅˆๅผ่…น่…”้ก็”จๅ™จๆขฐ
Risk Class 2
Cancelled

Registration Details

e272c3b521c771e819a77d48cbe3c054

DHA00601738508

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Oct 26, 2006

Oct 26, 2011

Nov 08, 2012

Cancellation Information

Logged out

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