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Bidi tuberculosis flora identification reagent (unsterilized) - Taiwan Registration bd4805ee84237d1e14682655b8045fbf

Access comprehensive regulatory information for Bidi tuberculosis flora identification reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd4805ee84237d1e14682655b8045fbf and manufactured by BECTON, DICKINSON AND COMPANY (BD). The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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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bd4805ee84237d1e14682655b8045fbf
Registration Details
Taiwan FDA Registration: bd4805ee84237d1e14682655b8045fbf
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Device Details

Bidi tuberculosis flora identification reagent (unsterilized)
TW: ๅฟ…ๅธ็ตๆ ธ่Œ็พค้‘‘ๅฎš่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

bd4805ee84237d1e14682655b8045fbf

DHA04400796501

Company Information

Product Details

Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.

C Immunology and microbiology

C.3370 ็ตๆ ธๆกฟ่Œๅ…็–ซ่žขๅ…‰่ฉฆๅŠ‘

import

Dates and Status

Aug 05, 2009

Aug 05, 2019

Jun 07, 2022

Cancellation Information

Logged out

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