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"Pacific" Sputum Collector (Sterilization) - Taiwan Registration 3b907c3cfc4860dfb08d0d06ab15faa3

Access comprehensive regulatory information for "Pacific" Sputum Collector (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3b907c3cfc4860dfb08d0d06ab15faa3 and manufactured by Pacific Medical Materials Co., Ltd. Copper Factory. The authorized representative in Taiwan is PACIFIC HOSPITAL SUPPLY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Pacific Medical Materials Co., Ltd. Copper Factory, and 2 recent registrations in the same category. 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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3b907c3cfc4860dfb08d0d06ab15faa3
Registration Details
Taiwan FDA Registration: 3b907c3cfc4860dfb08d0d06ab15faa3
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Device Details

"Pacific" Sputum Collector (Sterilization)
TW: โ€œๅคชๅนณๆด‹โ€ ็—ฐๆถฒๆ”ถ้›†ๅ™จ (ๆป…่Œ)
Risk Class 1

Registration Details

3b907c3cfc4860dfb08d0d06ab15faa3

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 22, 2016

Jul 22, 2026

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