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“RegenLab”RegenACR-C Classic Type III - Taiwan Registration 0fe1e8739d7f4eac17a6b9fbe0dc279b

Access comprehensive regulatory information for “RegenLab”RegenACR-C Classic Type III in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0fe1e8739d7f4eac17a6b9fbe0dc279b and manufactured by REGEN LAB SA. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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0fe1e8739d7f4eac17a6b9fbe0dc279b
Registration Details
Taiwan FDA Registration: 0fe1e8739d7f4eac17a6b9fbe0dc279b
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Device Details

“RegenLab”RegenACR-C Classic Type III
TW: “利奇”艾奇爾經典第三型血球細胞分離套組
Risk Class 2
MD

Registration Details

0fe1e8739d7f4eac17a6b9fbe0dc279b

Ministry of Health Medical Device Import No. 032418

DHA05603241803

Company Information

Switzerland

Product Details

This product is suitable for the preparation of Platelet-rich plasma (PRP), which can be used to treat chronic wounds.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Imported from abroad

Dates and Status

May 03, 2019

May 03, 2024