Taiwan FDA registration 1eb4d0373cbe0a52293be62345540338

Venice 伸縮OK繃 (未滅菌)

Taiwan·Risk Class 1·VENICE LABORATORIES CO., LTD.·Registered Oct 30, 2005 – Oct 30, 2025Expired

Registration details

Analysis ID: 1eb4d0373cbe0a52293be62345540338
Customs Code: DHY04300056001

Company information

Manufacturer: VENICE LABORATORIES CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: VENICE LABORATORIES CO., LTD.

Product details

Intended Use: It is used to cover and protect the wound and to join the skin wound. Not suitable for severe burns (grade 3).
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5240 Adhesive tapes and adhesive bandages for medical use
Import Information: Domestic

Dates and status

Registration Date: Oct 30, 2005
Expiry Date: Oct 30, 2025

About this record

Access comprehensive regulatory information for Venice 伸縮OK繃 (未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1eb4d0373cbe0a52293be62345540338 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES 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.