Taiwan FDA registration 5920a2c7be7fc546637737954d9b135a
“Genoss” GENOSS Control Syringe
TW: “吉諾司” 可控式顯影注射器
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Nov 01, 2021 – Nov 01, 2026ActiveRegistration details
- Analysis ID
- 5920a2c7be7fc546637737954d9b135a
- License Form
- Ministry of Health Medical Device Import No. 035016
- Customs Code
- DHA05603501601
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1650 Vascular photography syringes and syringes
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 01, 2021
- Expiry Date
- Nov 01, 2026
About this record
Access comprehensive regulatory information for “Genoss” GENOSS Control Syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5920a2c7be7fc546637737954d9b135a and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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