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"Keller" breast prosthesis booster delivery bag (sterilized) - Taiwan Registration a2d882b89f1c8848e589d0495669ae65

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 a2d882b89f1c8848e589d0495669ae65 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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a2d882b89f1c8848e589d0495669ae65
Registration Details
Taiwan FDA Registration: a2d882b89f1c8848e589d0495669ae65
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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

a2d882b89f1c8848e589d0495669ae65

DHA04401222800

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

Input;; QMS/QSD

Dates and Status

Oct 05, 2012

Oct 05, 2017

Jan 02, 2018

Cancellation Information

Logged out

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