Taiwan FDA registration db354441a26e427b152dc4207db7e559
"Gies Esme" plasma knife head
TW: “吉斯 愛斯美”電漿刀刀頭
Taiwan·Risk Class 2·GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.·Registered May 01, 2012 – May 01, 2017CancelledRegistration details
- Analysis ID
- db354441a26e427b152dc4207db7e559
- Customs Code
- DHA00602355608
Company information
- Manufacturer Country
- United States
- Authorized Representative
- MEDFRONT MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2012
- Expiry Date
- May 01, 2017
- Cancellation Date
- Nov 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Gies Esme" plasma knife head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db354441a26e427b152dc4207db7e559 and manufactured by GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices