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"Weishi" general surgery manual instrument (unsterilized) - Taiwan Registration d450eb3f16ea3f3f5a19695856eb1198

Access comprehensive regulatory information for "Weishi" general surgery manual instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d450eb3f16ea3f3f5a19695856eb1198 and manufactured by WISE MEDICAL CO. The authorized representative in Taiwan is HOME YOUR CORPORATION.

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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d450eb3f16ea3f3f5a19695856eb1198
Registration Details
Taiwan FDA Registration: d450eb3f16ea3f3f5a19695856eb1198
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Device Details

"Weishi" general surgery manual instrument (unsterilized)
TW: โ€œๅจๅฃซโ€ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d450eb3f16ea3f3f5a19695856eb1198

DHA04401102201

Company Information

Pakistan

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 04, 2011

Nov 04, 2016

Apr 25, 2018

Cancellation Information

Logged out

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