"Guise" all-titanium, all-artificial hearing ossicle replacement
Taiwan·Risk Class 2·GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.·Registered May 02, 2007 – May 02, 2017Cancelled- Analysis ID
- b27ed569d832c8415fa63951a08cd8be
- Customs Code
- DHA00601805100
- Manufacturer Country
- United States
- Authorized Representative
- MEDFRONT MEDICAL TECHNOLOGY CORPORATION
- 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.3495 Whole-hearing ossicle exchange
- Import Information
- import
- Registration Date
- May 02, 2007
- Expiry Date
- May 02, 2017
- Cancellation Date
- Nov 20, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
Access comprehensive regulatory information for "Guise" all-titanium, all-artificial hearing ossicle replacement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b27ed569d832c8415fa63951a08cd8be 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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