Taiwan FDA registration 3b907c3cfc4860dfb08d0d06ab15faa3

"Pacific" Sputum Collector (Sterilization)

TW: “太平洋” 痰液收集器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Jul 22, 2016 – Jul 22, 2026Expired
Registration details
Analysis ID
3b907c3cfc4860dfb08d0d06ab15faa3
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
PACIFIC HOSPITAL SUPPLY CO., LTD.
Product details
Intended Use
Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.2900 Microbial sample collection and delivery equipment
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Jul 22, 2016
Expiry Date
Jul 22, 2026
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About this record

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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