Skip to content

Vital Signs™ Pediatric Nasal CO2 Sampling with O2 Delivery Cannula for CapnoFlex Module

by AirLife Finland Oy

Ref 2013066-005

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10190752110595 Basic UDI-DI 10190752110595UDI-DIDate2 Dec 2021RegisteredStatusWithdrawn No longer placed on the EU market
United StatesGUDID listing GUDID Number10190752110595 UDI-DI Date27 Nov 2020ListedStatusListed GUDID: not 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  • Withdrawn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  • European Union CE/MDD Withdrawn
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Vital Signs™ Pediatric Nasal CO2 Sampling with O2 Delivery Cannula for CapnoFlex Module EUDAMED
Vital Signs™ GUDID
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling
Device Name
Vital Signs™ Gas monitoring
Model / Ref / Catalog
2013066-005
Primary DI / UDI-DI
10190752110595
Basic UDI-DI
B-10190752110595
FDA Product Code
CAT
EMDN Code
Z1203020485 Gaseous exchange monitoring instruments - consumables
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
868.5340
EU market of registration
Finland
GUDID distribution status
Not in Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I

Manufacturer details

EUDAMED SRN
FI-MF-000001482

Other devices from AirLife Finland Oy

See all devices from AirLife Finland Oy →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (17)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No