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MAINE FA RP2/RP2plus Control Panel(Non-Sterile) - Taiwan Registration 70e2acd14b56e12004ba5f33cda8a7ed

Access comprehensive regulatory information for MAINE FA RP2/RP2plus Control Panel(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 70e2acd14b56e12004ba5f33cda8a7ed and manufactured by Maine Molecular Quality Controls, Inc.. The authorized representative in Taiwan is DITECH ENTERPRISE 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.

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70e2acd14b56e12004ba5f33cda8a7ed
Registration Details
Taiwan FDA Registration: 70e2acd14b56e12004ba5f33cda8a7ed
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Device Details

MAINE FA RP2/RP2plus Control Panel(Non-Sterile)
TW: ้บฅๅฐผไบŒไปฃๅ‘ผๅธ้“ๅ“็ฎก่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

70e2acd14b56e12004ba5f33cda8a7ed

Ministry of Health Medical Device Import No. 021304

DHA09402130400

Company Information

Product Details

Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Feb 21, 2020

Feb 21, 2025