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0702045023

by Stryker Corp.

Ref 0702-045-023Model 08858251003190SR

0702045023 (0702-045-023) is a device classified as Class I in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 08858251003190SR) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 07613154881963), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251003190SR Basic UDI-DI 07613154881963UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613154881963 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251003190SR registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 07613154881963 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613154881963
  2. Registered EUDAMED 08858251003190SR

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  • Withdrawn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

Generic name
Surgical fluid/smoke waste management system
Device name
Neptune Smoke Tubing
Model / Ref / Catalog
08858251003190SR, 0702-045-023, 0702045023
Primary DI / UDI-DI
07613154881963
Basic UDI-DI
08858251003190SR
FDA product code
JCX
EMDN code
Z12019085 Various instruments for general and multidisciplinary surgery - consumables
GMDN term
Surgical fluid/smoke waste management system
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4780
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858251003190SR
0702-045-023
GUDID
0702045023
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Surgical fluid/smoke waste management system

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - CONSUMABLES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)