Taiwan FDA registration 5d95772989f102b6db914e7cc89c46f8

Novo pen microneedling

TW: 諾和筆微針

Taiwan·Risk Class 2·NOVO NORDISK A/S;; NIPRO MEDICAL INDUSTRIES LTD., TATEBAYASHI PLANT·Registered Jul 16, 2024 – Jul 16, 2029Active

Registration details

Analysis ID: 5d95772989f102b6db914e7cc89c46f8
Customs Code: DHA05603725105

Company information

Manufacturer: NOVO NORDISK A/S;; NIPRO MEDICAL INDUSTRIES LTD., TATEBAYASHI PLANT
Manufacturer Country: Japan;;Denmark
Authorized Representative: NOVO NORDISK PHARMA (TAIWAN) LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5570 Subcutaneous single-chamber needle
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Jul 16, 2024
Expiry Date: Jul 16, 2029

About this record

Access comprehensive regulatory information for Novo pen microneedling in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5d95772989f102b6db914e7cc89c46f8 and manufactured by NOVO NORDISK A/S;; NIPRO MEDICAL INDUSTRIES LTD., TATEBAYASHI PLANT. The authorized representative in Taiwan is NOVO NORDISK PHARMA (TAIWAN) LTD..

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