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"Meidi" manual instrument for general surgery (unsterilized) - Taiwan Registration c690e8711a5511b1c835fdd82b171084

Access comprehensive regulatory information for "Meidi" manual instrument 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 c690e8711a5511b1c835fdd82b171084 and manufactured by MEDE TECHNIK. The authorized representative in Taiwan is AK INSTRUMENTS 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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c690e8711a5511b1c835fdd82b171084
Registration Details
Taiwan FDA Registration: c690e8711a5511b1c835fdd82b171084
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Device Details

"Meidi" manual instrument for general surgery (unsterilized)
TW: "ๆข…่ฟช" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c690e8711a5511b1c835fdd82b171084

DHA04401146305

Company Information

Germany

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

Mar 14, 2012

Mar 14, 2022

Apr 12, 2024

Cancellation Information

Logged out

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