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"Keller" breast prosthesis booster delivery bag (sterilized) - Taiwan Registration 65459e9f739935c8ba0dbbc90d12d790

Access comprehensive regulatory information for "Keller" breast prosthesis booster delivery bag (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65459e9f739935c8ba0dbbc90d12d790 and manufactured by KELLER MEDICAL , INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KELLER MEDICAL , INC., and 1 recent registrations in the same category. 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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65459e9f739935c8ba0dbbc90d12d790
Registration Details
Taiwan FDA Registration: 65459e9f739935c8ba0dbbc90d12d790
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Device Details

"Keller" breast prosthesis booster delivery bag (sterilized)
TW: โ€œๅ‡ฑๅ‹’โ€็พฉไนณ่ผ”ๅŠฉ้ž้€่ข‹ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

65459e9f739935c8ba0dbbc90d12d790

DHA09401864207

Company Information

United States

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 22, 2017

Dec 22, 2022

Apr 12, 2024

Cancellation Information

Logged out

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