"Keller" breast prosthesis booster delivery bag (sterilized)
Taiwan·Risk Class 1·KELLER MEDICAL , INC.·Registered Oct 05, 2012 – Oct 05, 2017Cancelled- Analysis ID
- a2d882b89f1c8848e589d0495669ae65
- Customs Code
- DHA04401222800
- Manufacturer
- KELLER MEDICAL , INC.
- Manufacturer Country
- United States
- Authorized Representative
- ICARES MEDICUS, INC.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; QMS/QSD
- Registration Date
- Oct 05, 2012
- Expiry Date
- Oct 05, 2017
- Cancellation Date
- Jan 02, 2018
- Status
- Logged out
- Reason
- 自請註銷;;許可證已逾有效期
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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.