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"Ya'Arth" medical light source machine - Taiwan Registration fb3ac20a73042731190f0d837ee90bb5

Access comprehensive regulatory information for "Ya'Arth" medical light source machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb3ac20a73042731190f0d837ee90bb5 and manufactured by AESCULAP AG. The authorized representative in Taiwan is Taiwan Birlanc Co., 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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fb3ac20a73042731190f0d837ee90bb5
Registration Details
Taiwan FDA Registration: fb3ac20a73042731190f0d837ee90bb5
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Device Details

"Ya'Arth" medical light source machine
TW: "้›…ๆฐ" ้†ซ็”จๅ…‰ๆบๆฉŸ
Risk Class 2
Cancelled

Registration Details

fb3ac20a73042731190f0d837ee90bb5

DHA00601359308

Company Information

Germany

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

Nov 18, 2005

Nov 18, 2020

Jul 15, 2022

Cancellation Information

Logged out

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