Novo Pen Yierle
Taiwan·Risk Class 2·Novo Nordisk A/S, Device Manufacturing Development·Registered Mar 20, 2020 – Apr 28, 2021Cancelled- Analysis ID
- f1cb8f937bd1ce37fe9343a10952dba8
- Customs Code
- DHA00602229106
- Manufacturer Country
- Denmark
- Authorized Representative
- NOVO NORDISK PHARMA (TAIWAN) LTD.
- 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)
- J.6920 注射針導引器
- Import Information
- import
- Registration Date
- Mar 20, 2020
- Expiry Date
- Apr 28, 2021
- Cancellation Date
- Aug 18, 2023
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.