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Revmed TriCeLL PRP KIT - Taiwan Registration 5ce85a4461481a7423e36280ea0faedd

Access comprehensive regulatory information for Revmed TriCeLL PRP KIT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ce85a4461481a7423e36280ea0faedd and manufactured by REV-MED, Inc.. The authorized representative in Taiwan is AUGUSMED BIOTECH INC..

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.

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5ce85a4461481a7423e36280ea0faedd
Registration Details
Taiwan FDA Registration: 5ce85a4461481a7423e36280ea0faedd
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Device Details

Revmed TriCeLL PRP KIT
TW: โ€œ่Šฎๆธผโ€ โ€œไธ‰็”ฐโ€ ่ก€็ƒ็ดฐ่ƒžๅˆ†้›ข็ต„
Risk Class 2
MD

Registration Details

5ce85a4461481a7423e36280ea0faedd

Ministry of Health Medical Device Import No. 028448

DHA05602844800

Company Information

Korea, Republic of

Product Details

When this product is used, blood is removed from the patient, and an autologous platelet concentrate (PRP) is prepared by a secondary centrifugation procedure. When clinically indicated, autologous platelet concentrate can be mixed with bone implants (Bone graft) or used alone at orthopedic surgical sites.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Imported from abroad

Dates and Status

Jun 22, 2016

Jun 22, 2021