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"Libao" inspection brush (sterilized/unsterilized) - Taiwan Registration e2e0904ce30e7c0d24fb05a0a063541e

Access comprehensive regulatory information for "Libao" inspection brush (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e2e0904ce30e7c0d24fb05a0a063541e and manufactured by Taiwan Libao Medical Equipment Co., Ltd. The authorized representative in Taiwan is LIBO MEDICAL PRODUCTS INC..

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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e2e0904ce30e7c0d24fb05a0a063541e
Registration Details
Taiwan FDA Registration: e2e0904ce30e7c0d24fb05a0a063541e
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Device Details

"Libao" inspection brush (sterilized/unsterilized)
TW: โ€œ็ซ‹ๅฏถโ€ๆŽกๆชขๅˆท(ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e2e0904ce30e7c0d24fb05a0a063541e

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.

C Immunology and microbiology

C.2900 Microbial sample collection and delivery equipment

Domestic

Dates and Status

Aug 28, 2012

Aug 28, 2027