Taiwan FDA registration 09ef46011535c80cf90c3bf717150009
NordiFlex PenMate
TW: 諾易筆筆伴
Taiwan·Risk Class 2·MD·Novo Nordisk A/S·Registered Feb 27, 2019 – Feb 27, 2024ExpiredRegistration details
- Analysis ID
- 09ef46011535c80cf90c3bf717150009
- License Form
- Ministry of Health Medical Device Import No. 032276
- Customs Code
- DHA05603227609
Company information
- Manufacturer
- Novo Nordisk A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- NOVO NORDISK PHARMA (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5860 piston syringe barrel
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 27, 2019
- Expiry Date
- Feb 27, 2024
About this record
Access comprehensive regulatory information for NordiFlex PenMate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09ef46011535c80cf90c3bf717150009 and manufactured by Novo Nordisk A/S. The authorized representative in Taiwan is NOVO NORDISK PHARMA (TAIWAN) LTD..
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