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"Red" endotracheal probe (unsterilized) - Taiwan Registration 1f295967bb406b6f0a82cd52489d67f8

Access comprehensive regulatory information for "Red" endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f295967bb406b6f0a82cd52489d67f8 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is Xin Yi Limited.

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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1f295967bb406b6f0a82cd52489d67f8
Registration Details
Taiwan FDA Registration: 1f295967bb406b6f0a82cd52489d67f8
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Device Details

"Red" endotracheal probe (unsterilized)
TW: "้›ทๅพท" ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1f295967bb406b6f0a82cd52489d67f8

DHA04400324400

Company Information

Norway

Product Details

It is limited to the first level of identification scope of the Administrative Measures for Medical Devices (endotracheal tube probe [D.5790]).

D Anesthesiology

import

Dates and Status

Mar 29, 2006

Mar 29, 2011

Nov 23, 2012

Cancellation Information

Logged out

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