Taiwan FDA registration d8cb14f0836a0be38fcaebfd45b54eaa
“Genoss” GENOSS Inflator B30 and GENOSS Inflator B40
TW: “吉諾司” 擴張壓力泵
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Nov 01, 2021 – Nov 01, 2026ActiveRegistration details
- Analysis ID
- d8cb14f0836a0be38fcaebfd45b54eaa
- License Form
- Ministry of Health Medical Device Import No. 035017
- Customs Code
- DHA05603501700
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 Inflator B30 and GENOSS Inflator B40 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8cb14f0836a0be38fcaebfd45b54eaa and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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