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"Bluepoint" Airway connector (Non-Sterile) - Taiwan Registration 088f69e3d8f29bcb4b660506c18b8af7

Access comprehensive regulatory information for "Bluepoint" Airway connector (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 088f69e3d8f29bcb4b660506c18b8af7 and manufactured by BLUEPOINT MEDICAL GMBH & CO KG. The authorized representative in Taiwan is ELC ENTERPRISE 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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088f69e3d8f29bcb4b660506c18b8af7
Registration Details
Taiwan FDA Registration: 088f69e3d8f29bcb4b660506c18b8af7
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Device Details

"Bluepoint" Airway connector (Non-Sterile)
TW: "ๅธƒ้ญฏๆณข้Ÿณ" ๆฐฃ้“้€ฃๆŽฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

088f69e3d8f29bcb4b660506c18b8af7

Ministry of Health Medical Device Import No. 013888

DHA09401388801

Company Information

Product Details

D Devices for anesthesiology

D5810 airway connector

Imported from abroad

Dates and Status

Feb 26, 2014

Feb 26, 2019

Aug 05, 2022

Cancellation Information

Logged out

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