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"LDBIO Diagnostics" Aspergillus Assay (Non-sterile) - Taiwan Registration af7d7eb926018ff499d1a21ad7d94dae

Access comprehensive regulatory information for "LDBIO Diagnostics" Aspergillus Assay (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 af7d7eb926018ff499d1a21ad7d94dae and manufactured by LDBIO DIAGNOSTICS. The authorized representative in Taiwan is RECHI CO., LTD..

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af7d7eb926018ff499d1a21ad7d94dae
Registration Details
Taiwan FDA Registration: af7d7eb926018ff499d1a21ad7d94dae
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Device Details

"LDBIO Diagnostics" Aspergillus Assay (Non-sterile)
TW: "ๅ‹ž่ฟชๆ‹œ็ˆพ" ้บด่Œๅฑฌๆชขๆธฌๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

af7d7eb926018ff499d1a21ad7d94dae

Ministry of Health Medical Device Import No. 020790

DHA09402079001

Company Information

France

Product Details

Limited to the first level identification range of koji seroreagent (C.3040) of the measures for the administration of medical equipment.

C Immunology and microbiology devices

C3040 Koji seroreagent

Imported from abroad

Dates and Status

Aug 27, 2019

Aug 27, 2024