Taiwan FDA registration 62643e45cee11a4f95494390efb12a35

"Menick" Skin Pressure Protector (Non-Sterilized)

TW: "墨尼克" 皮膚壓力保護器 (未滅菌)

Taiwan·Risk Class 1·Mölnlycke Manufacturing US, LLC·Registered Jun 21, 2024 – Oct 31, 2025Expired

Registration details

Analysis ID: 62643e45cee11a4f95494390efb12a35
Customs Code: DHA084A0028602

Company information

Manufacturer: Mölnlycke Manufacturing US, LLC
Manufacturer Country: United States
Authorized Representative: MOLNLYCKE HEALTH CARE TAIWAN CO., LTD.

Product details

Intended Use: It is limited to the scope of the first level of identification of skin pressure protectors (J.6450) in the classification and grading management measures for medical devices.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6450 Skin Pressure Protector
Import Information: import

Dates and status

Registration Date: Jun 21, 2024
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for "Menick" Skin Pressure Protector (Non-Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 62643e45cee11a4f95494390efb12a35 and manufactured by Mölnlycke Manufacturing US, LLC. The authorized representative in Taiwan is MOLNLYCKE HEALTH CARE TAIWAN 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.