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"ACRO" Adenovirus test kit (Non-Sterile) - Taiwan Registration 67f5998385d4e52d24ded91156a40c2b

Access comprehensive regulatory information for "ACRO" Adenovirus test kit (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 67f5998385d4e52d24ded91156a40c2b and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH 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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67f5998385d4e52d24ded91156a40c2b
Registration Details
Taiwan FDA Registration: 67f5998385d4e52d24ded91156a40c2b
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Device Details

"ACRO" Adenovirus test kit (Non-Sterile)
TW: "ๆ„›ๅฏ็พ…" ่…บ็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

67f5998385d4e52d24ded91156a40c2b

Ministry of Health Medical Device Import No. 019236

DHA09401923601

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".

C Immunology and microbiology devices

C3020 adenovirus serum reagent

Imported from abroad

Dates and Status

Jun 26, 2018

Jun 26, 2028