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"ACRO" Mycoplasma Pneumoniae Test (Non-sterile) - Taiwan Registration 5ac273ec228fa150946efa9b07019d59

Access comprehensive regulatory information for "ACRO" Mycoplasma Pneumoniae 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 5ac273ec228fa150946efa9b07019d59 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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5ac273ec228fa150946efa9b07019d59
Registration Details
Taiwan FDA Registration: 5ac273ec228fa150946efa9b07019d59
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Device Details

"ACRO" Mycoplasma Pneumoniae Test (Non-sterile)
TW: "ๆ„›ๅฏ็พ…" ่‚บ็‚Ž้ปดๆผฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5ac273ec228fa150946efa9b07019d59

Ministry of Health Medical Device Import No. 017392

DHA09401739205

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".

C Immunology and microbiology devices

C3375 Mycoplasma serum reagent

Imported from abroad

Dates and Status

Jan 10, 2017

Jan 10, 2027