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"Lucelen" Manual instruments for general surgery (unsterilized) - Taiwan Registration 970a492413e3e6fb31a5f7776fa1ec97

Access comprehensive regulatory information for "Lucelen" 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 970a492413e3e6fb31a5f7776fa1ec97 and manufactured by AUGUST REUCHLEN GMBH. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, INC..

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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970a492413e3e6fb31a5f7776fa1ec97
Registration Details
Taiwan FDA Registration: 970a492413e3e6fb31a5f7776fa1ec97
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Device Details

"Lucelen" Manual instruments for general surgery (unsterilized)
TW: "่ทฏๆ–ฏๅ€ซ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

970a492413e3e6fb31a5f7776fa1ec97

DHA04401145009

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 08, 2012

Mar 08, 2022

Apr 12, 2024

Cancellation Information

Logged out

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