Pure Global
Taiwan FDA registration 760719c5b711ec64ea0f6f3f04c9120b

Nord pen companion

TW: 諾德筆伴
Taiwan flagTaiwan·Risk Class 2·NOVO NORDISK A/S DEVICE MANUFACTURING DEVELOPMENT·Registered Sep 14, 2005 – Sep 14, 2020Cancelled
Registration details
Analysis ID
760719c5b711ec64ea0f6f3f04c9120b
Customs Code
DHA00601190109
Company information
Manufacturer
NOVO NORDISK A/S DEVICE MANUFACTURING DEVELOPMENT
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
Import Information
import
Dates and status
Registration Date
Sep 14, 2005
Expiry Date
Sep 14, 2020
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for Nord pen companion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 760719c5b711ec64ea0f6f3f04c9120b and manufactured by NOVO NORDISK A/S DEVICE MANUFACTURING DEVELOPMENT. The authorized representative in Taiwan is NOVO NORDISK PHARMA (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices