Taiwan FDA registration 3781bc7787f70c957590840ca5bd9cd5

"Pajik" Manual instruments for general surgery (unsterilized)

TW: "帕將克" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Apr 06, 2011 – Apr 06, 2026Expired

Registration details

Analysis ID: 3781bc7787f70c957590840ca5bd9cd5
Customs Code: DHA04401014206

Company information

Manufacturer: PAJUNK GMBH MEDIZINTECHNOLOGIE
Manufacturer Country: Germany
Authorized Representative: Huizhong Co., Ltd

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Apr 06, 2011
Expiry Date: Apr 06, 2026

About this record

Access comprehensive regulatory information for "Pajik" Manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3781bc7787f70c957590840ca5bd9cd5 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., 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.