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7-Ft Adult Nasal Pressure Monitoring Cannula w/ filter (Box of 50)

by S.L.P. Ltd.

Ref 15805-FT-50Model 158XX series

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None, self-declared

Class I: no certifier involved

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 Number7290013385PR002VD Basic UDI-DI 07290013817617UDI-DIDate27 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number07290013817617 UDI-DI Date1 Jun 2022ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 25 Oct 2026.

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  • Withdrawn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
7-Ft Adult Nasal Pressure Monitoring Cannula w/ filter (Box of 50) EUDAMED
SleepSense GUDID
Generic Name
Respiratory oxygen sensor
Device Name
Pressure Sampling Cannulas and Transducer Protector
Model / Reference
158XX series, 15805-FT-50
Primary DI / UDI-DI
07290013817617
Basic UDI-DI
7290013385PR002VD
510(k) Number
FDA Product Code
MNR
EMDN Code
Z1399 Non-specific consumables for diagnostic instruments - other
GMDN Term
Respiratory oxygen sensor
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
868.2375
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
IL-MF-000016600
Authorised representative
Arazy Group GmbH DE-AR-000007685

Other devices from S.L.P. Ltd.

See all devices from S.L.P. Ltd. →

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (20)

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