Pure Global
Taiwan FDA registration 7fbb6005b8a237ea2b96c07431a3737b

Nord Pen 10

TW: 諾德筆 10
Taiwan flagTaiwan·Risk Class 2·Novo Nordisk A/S, Device Manufacturing Development·Registered Jun 03, 2005 – Jun 03, 2020Cancelled
Registration details
Analysis ID
7fbb6005b8a237ea2b96c07431a3737b
Customs Code
DHA00601135801
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
Jun 03, 2005
Expiry Date
Jun 03, 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 10 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fbb6005b8a237ea2b96c07431a3737b 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