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"Pacific" closed suction sleeve (sterilized) - Taiwan Registration a40281a3d019696899398a489d8ead19

Access comprehensive regulatory information for "Pacific" closed suction sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a40281a3d019696899398a489d8ead19 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. 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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a40281a3d019696899398a489d8ead19
Registration Details
Taiwan FDA Registration: a40281a3d019696899398a489d8ead19
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Device Details

"Pacific" closed suction sleeve (sterilized)
TW: โ€œๅคชๅนณๆด‹โ€ๅฏ†้–‰ๅผๆŠฝ็—ฐๅฅ— (ๆป…่Œ)
Risk Class 1

Registration Details

a40281a3d019696899398a489d8ead19

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Jul 11, 2006

Jul 11, 2026