Taiwan FDA registration 7b7781d83bd15290914ccf0a2520f691

Novo Pen Yierle

TW: 諾和筆易兒樂
Taiwan flagTaiwan·Risk Class 2·NOVO NORDISK A/S;; NOVO NORDISK (CHINA) PHARMACEUTICALS CO., LTD.·Registered Mar 10, 2016 – Mar 10, 2026Expired
Registration details
Analysis ID
7b7781d83bd15290914ccf0a2520f691
Customs Code
DHA09200072909
Company information
Manufacturer Country
China;;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
Product Type (Level 2)
J.6920 注射針導引器
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Mar 10, 2016
Expiry Date
Mar 10, 2026
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About this record

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 7b7781d83bd15290914ccf0a2520f691 and manufactured by NOVO NORDISK A/S;; NOVO NORDISK (CHINA) PHARMACEUTICALS CO., LTD.. 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, Device Manufacturing Development, 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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