Taiwan FDA registration 1dfe3d14785671509f0431943b24a40b

"Menick" Mepilet waterproof post-operative silver dressing

TW: “墨尼克”美皮蕾防水型術後銀敷料
Taiwan flagTaiwan·Risk Class 2·Mölnlycke Health Care AB; Mölnlycke Health Care Oy·Registered Jun 27, 2019 – Jun 27, 2024Expired
Registration details
Analysis ID
1dfe3d14785671509f0431943b24a40b
Customs Code
DHA05603270802
Company information
Manufacturer Country
Finland;;Sweden
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4018 親水性創傷覆蓋材
Import Information
import
Dates and status
Registration Date
Jun 27, 2019
Expiry Date
Jun 27, 2024
About this record

Access comprehensive regulatory information for "Menick" Mepilet waterproof post-operative silver dressing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1dfe3d14785671509f0431943b24a40b and manufactured by Mölnlycke Health Care AB; Mölnlycke Health Care Oy. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices