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"Artima" manual instruments for general surgery (unsterilized) - Taiwan Registration b632f639179c0b88543e30a696d9e0d1

Access comprehensive regulatory information for "Artima" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b632f639179c0b88543e30a696d9e0d1 and manufactured by ULTIMATE MEDICAL PRODUCTS LTD.. The authorized representative in Taiwan is Liren Equipment Factory 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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b632f639179c0b88543e30a696d9e0d1
Registration Details
Taiwan FDA Registration: b632f639179c0b88543e30a696d9e0d1
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Device Details

"Artima" manual instruments for general surgery (unsterilized)
TW: โ€œ้˜ฟ็ทน็‘ชโ€ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b632f639179c0b88543e30a696d9e0d1

DHA04400632400

Company Information

United Arab Emirates

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Nov 27, 2007

Nov 27, 2012

Apr 16, 2014

Cancellation Information

Logged out

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