“Genoss” Osteon
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered May 29, 2014 – May 29, 2024Cancelled- Analysis ID
- b591e09acb94c427f6540c09ba08041c
- License Form
- Ministry of Health Medical Device Import No. 026185
- Customs Code
- DHA05602618507
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MRS MICRO-WORK COMPANY LIMITED
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3930 Tricalcium phosphate for alveolar bone restoration
- Import Information
- Imported from abroad
- Registration Date
- May 29, 2014
- Expiry Date
- May 29, 2024
- Cancellation Date
- Jun 05, 2023
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for “Genoss” Osteon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b591e09acb94c427f6540c09ba08041c and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is MRS MICRO-WORK COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Genoss Co., Ltd., and 1 recent registrations in the same category. 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.