Taiwan FDA registration 583d85aba45fc6aa95b05cfeb8c48560
“Genoss” Polymer Guide(Non-sterile)
TW: “吉諾斯”牙科手術用指示器 (未滅菌)
Taiwan·Risk Class 1·MD·Genoss Co., Ltd.·Registered Oct 16, 2013 – Oct 16, 2023CancelledRegistration details
- Analysis ID
- 583d85aba45fc6aa95b05cfeb8c48560
- License Form
- Ministry of Health Medical Device Import No. 013506
- Customs Code
- DHA09401350600
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MRS MICRO-WORK COMPANY LIMITED
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 16, 2013
- Expiry Date
- Oct 16, 2023
- Cancellation Date
- Jun 13, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請廢止
About this record
Access comprehensive regulatory information for “Genoss” Polymer Guide(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 583d85aba45fc6aa95b05cfeb8c48560 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is MRS MICRO-WORK COMPANY LIMITED.
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