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Pentax Manual Instruments for Surgery (Unsterilized) - Taiwan Registration 765b6485379774d0aeb71a61c9d36c55

Access comprehensive regulatory information for Pentax Manual Instruments for 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 765b6485379774d0aeb71a61c9d36c55 and manufactured by PENTAX CORPORATION. The authorized representative in Taiwan is WHOLE WELL 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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765b6485379774d0aeb71a61c9d36c55
Registration Details
Taiwan FDA Registration: 765b6485379774d0aeb71a61c9d36c55
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Device Details

Pentax Manual Instruments for Surgery (Unsterilized)
TW: โ€œ่ณ“ๅพ—ๅฃซโ€ๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

765b6485379774d0aeb71a61c9d36c55

DHA04400433801

Company Information

Japan

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

May 04, 2006

May 04, 2011

Jul 25, 2014

Cancellation Information

Logged out

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