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Libocai brush inspection group (sterilized/unsterilized) - Taiwan Registration 8db1a529c8f8164eb01df0f0b654e693

Access comprehensive regulatory information for Libocai brush inspection group (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 8db1a529c8f8164eb01df0f0b654e693 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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8db1a529c8f8164eb01df0f0b654e693
Registration Details
Taiwan FDA Registration: 8db1a529c8f8164eb01df0f0b654e693
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Device Details

Libocai brush inspection group (sterilized/unsterilized)
TW: ็ซ‹ๅฏถๆŽกๆชขๅˆท็ต„(ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8db1a529c8f8164eb01df0f0b654e693

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

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Jul 15, 2009

Jul 15, 2029