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Nasal Cannula, CO2 Sampling line, male luer, infant

by Besmed Health Business Corp.

Ref NC-87500

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

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-NC-87500Y2 Basic UDI-DI D-NC-87500Y2UDI-DIDate4 May 2022RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-NC-87500Y2 UDI-DI Date7 Sep 2016ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Nasal Cannula, CO2 Sampling line, male luer, infant EUDAMED
Oxygen Nasal Cannula Infant,W/co2 Sampling line(Male Luer) GUDID
Generic Name
Oxygen administration tubing
Device Name
Nasal Cannula, 7Ft Tube, CO2 Sampling line, Male luer, Infant
Model / Reference
NC-87500
Primary DI / UDI-DI
D-NC-87500Y2 EUDAMED
04716770875002 GUDID
Basic UDI-DI
B-NC-87500Y2
510(k) Number
FDA Product Code
CCK
EMDN Code
R03010207 Oxygen therapy kits
GMDN Term
Oxygen administration tubing
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
868.1400
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D-NC-87500Y2
GUDID
04716770875002
Device ClassEUDAMED
Class IIa
GUDID
Class II
Contains LatexEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
TW-MF-000007246
Authorised representative
mdi Europa GmbH DE-AR-000006218

Other devices from Besmed Health Business Corp.

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Properties

  • Single Use
  • Contains Latex NoEUDAMEDYesGUDID
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (16)

  • Sterile: No
  • Implantable: No
  • Reusable: 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
  • Premarket Exempt: No
  • Serial Number: No