Taiwan FDA registration 7a075493a0522037301b02e7167fc397
“Gyrus”Prosthesis modification instrument for ossicular replacement surgery(Non-sterile)
TW: “吉洛氏”聽小骨置換物修正用器械 (未滅菌)
Taiwan·Risk Class 1·MD·GYRUS MEDICAL GMBH·Registered Mar 18, 2014 – Mar 18, 2019CancelledRegistration details
- Analysis ID
- 7a075493a0522037301b02e7167fc397
- License Form
- Ministry of Health Medical Device Import No. 013969
- Customs Code
- DHA09401396901
Company information
- Manufacturer
- GYRUS MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yuanyou Industrial Co., Ltd
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3540 Instrument for Hearing Bone Replacement Correction
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 18, 2014
- Expiry Date
- Mar 18, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Gyrus”Prosthesis modification instrument for ossicular replacement surgery(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7a075493a0522037301b02e7167fc397 and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is Yuanyou Industrial Co., Ltd.
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