Taiwan FDA registration a936f5161f1564551854135a9dfe6dd0

"Mireil" Plano titanium alloy non-absorbable fixtures

TW: “渼瑞爾”普朗鈦合金不可吸收固定裝置

Taiwan·Risk Class 2·Meril Endo Surgery Pvt. Ltd·Registered Oct 01, 2024 – Oct 01, 2029Active

Registration details

Analysis ID: a936f5161f1564551854135a9dfe6dd0
Customs Code: DHA05603761201

Company information

Manufacturer: Meril Endo Surgery Pvt. Ltd
Manufacturer Country: India
Authorized Representative: K&C MEDICAL CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4750 Implantable Joints
Import Information: import

Dates and status

Registration Date: Oct 01, 2024
Expiry Date: Oct 01, 2029

About this record

Access comprehensive regulatory information for "Mireil" Plano titanium alloy non-absorbable fixtures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a936f5161f1564551854135a9dfe6dd0 and manufactured by Meril Endo Surgery Pvt. Ltd. The authorized representative in Taiwan is K&C MEDICAL 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.