Taiwan FDA registration 00bfbded7c8571fe799ce3660291827d
"Guise" modular part artificial hearing ossicles
TW: “吉斯”模組式部分人工聽小骨
Taiwan·Risk Class 2·GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.·Registered May 01, 2007 – May 01, 2017CancelledRegistration details
- Analysis ID
- 00bfbded7c8571fe799ce3660291827d
- Customs Code
- DHA00601805008
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)
- G ENT Science
- Product Type (Level 2)
- G.3450 Partial ossicular exchange
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2007
- 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 "Guise" modular part artificial hearing ossicles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00bfbded7c8571fe799ce3660291827d and manufactured by GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
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