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"GE" water trap (Non-Sterile) - Taiwan Registration 42e020e303d4fed11a27f0e78214bf9d

Access comprehensive regulatory information for "GE" water trap (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42e020e303d4fed11a27f0e78214bf9d and manufactured by GE HEALTHCARE. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GE Healthcare, and 1 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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42e020e303d4fed11a27f0e78214bf9d
Registration Details
Taiwan FDA Registration: 42e020e303d4fed11a27f0e78214bf9d
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Device Details

"GE" water trap (Non-Sterile)
TW: "ๅฅ‡็•ฐ" ้›†ๆฐดๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

42e020e303d4fed11a27f0e78214bf9d

Ministry of Health Medical Device Import No. 016551

DHA09401655107

Company Information

Estonia

Product Details

Limited to the first level identification range of the "T-shaped drainage (water collector) (D.5995)" of the Measures for the Administration of Medical Equipment.

D Devices for anesthesiology

D5995 T-drain (water collector)

Imported from abroad

Dates and Status

May 18, 2016

May 18, 2026

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