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Nord Pen 10 - Taiwan Registration 7fbb6005b8a237ea2b96c07431a3737b

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.

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7fbb6005b8a237ea2b96c07431a3737b
Registration Details
Taiwan FDA Registration: 7fbb6005b8a237ea2b96c07431a3737b
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Device Details

Nord Pen 10
TW: ่ซพๅพท็ญ† 10
Risk Class 2
Cancelled

Registration Details

7fbb6005b8a237ea2b96c07431a3737b

DHA00601135801

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

import

Dates and Status

Jun 03, 2005

Jun 03, 2020

Jun 16, 2022

Cancellation Information

Logged out

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