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Airtraq A600B

by Prodol Meditec, Ltd.

Ref A600BModel Airtraq Plus Video Laryngoscope

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number069360261A60023 Basic UDI-DI 00693602616023UDI-DIDate24 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00693602616023 UDI-DI Date6 Nov 2025ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Airtraq Plus Video Laryngoscope Basic EUDAMED
Airtraq GUDID
Generic Name
Video intubation laryngoscope imaging system
Device Name
Airtraq Plus Video Laryngoscope
Model / Reference
A600B, Airtraq Plus Video Laryngoscope
Primary DI / UDI-DI
00693602616023
Basic UDI-DI
069360261A60023
Direct Marketing DI
00693602616016
FDA Product Code
CCW
EMDN Code
Z12021004 Video laryngoscopes
GMDN Term
Video intubation laryngoscope imaging system
Device Class
Class I
Regulation Number
868.5540
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Other devices from Prodol Meditec, Ltd.

See all devices from Prodol Meditec, Ltd. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No