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Novo Pen Yierle - Taiwan Registration f1cb8f937bd1ce37fe9343a10952dba8

Access comprehensive regulatory information for Novo Pen Yierle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f1cb8f937bd1ce37fe9343a10952dba8 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, 1 companies making similar products including NOVO NORDISK A/S;; NOVO NORDISK (CHINA) PHARMACEUTICALS CO., LTD., and 1 recent registrations in the same category. 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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f1cb8f937bd1ce37fe9343a10952dba8
Registration Details
Taiwan FDA Registration: f1cb8f937bd1ce37fe9343a10952dba8
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Device Details

Novo Pen Yierle
TW: ่ซพๅ’Œ็ญ†ๆ˜“ๅ…’ๆจ‚
Risk Class 2
Cancelled

Registration Details

f1cb8f937bd1ce37fe9343a10952dba8

DHA00602229106

Company Information

Product Details

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

J General hospital and personal use equipment

J.6920 ๆณจๅฐ„้‡ๅฐŽๅผ•ๅ™จ

import

Dates and Status

Mar 20, 2020

Apr 28, 2021

Aug 18, 2023

Cancellation Information

Logged out

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