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Airtraq

FDA UDI

Class I (US FDA UDI)

by Prodol Meditec , Ltd.

Identity

Trade Name
Airtraq FDA UDI
Generic Name
Video intubation laryngoscope blade/handle shell FDA UDI
Device Name
Airtraq Plus Video Laryngoscope Blade Channeled Pediatric Size 1 FDA UDI
Model / Reference
A6C1 FDA UDI
Description
Airtraq Plus Video Laryngoscope Blade Channeled Pediatric Size 1 FDA UDI

Identifiers

Primary DI / UDI-DI
00693602616115 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Video intubation laryngoscope blade/handle shell FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Video intubation laryngoscope blade/handle shell

Airtraq by Prodol Meditec , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Video intubation laryngoscope blade/handle shell.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Prodol Meditec , Ltd.

Sources (1)

  • FDA UDI daaa05df-cb10-4f9e-b114-b92d1037b721 33 fields · synced May 29, 2026