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"ACRO BIOTECH" Legionella-Ag test (Non-Sterile) - Taiwan Registration 734c6e0dde715a1c9c830efa224ba4b0

Access comprehensive regulatory information for "ACRO BIOTECH" Legionella-Ag test (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 734c6e0dde715a1c9c830efa224ba4b0 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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734c6e0dde715a1c9c830efa224ba4b0
Registration Details
Taiwan FDA Registration: 734c6e0dde715a1c9c830efa224ba4b0
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Device Details

"ACRO BIOTECH" Legionella-Ag test (Non-Sterile)
TW: "ๆ„›ๅฏ็พ…" ้€€ไผ่ปไบบ่‚บ็‚ŽๆŠ—ๅŽŸๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

734c6e0dde715a1c9c830efa224ba4b0

Ministry of Health Medical Device Import No. 021466

DHA09402146600

Company Information

United States

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology devices

C3300 Haemophilus serology

Imported from abroad

Dates and Status

Apr 17, 2020

Apr 17, 2025