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0702034000

by Stryker Corp.

Ref 0702-034-000Model 08858250000620RP

0702034000 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 08858250000620RP) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 07613154674930), 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 Number08858250000620RP Basic UDI-DI 07613154674930UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613154674930 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000620RP registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 07613154674930 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613154674930
  2. Registered EUDAMED 08858250000620RP

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  • Withdrawn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 Fluid Suction Filters
Model / Ref / Catalog
08858250000620RP EUDAMED
0702-034-000 EUDAMED
0702034000 GUDID
Primary DI / UDI-DI
07613154674930
Basic UDI-DI
08858250000620RP
Direct marketing DI
07613154674930
FDA product code
JCX
EMDN code
Z12019004 Surgical smoke evacuation systems
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
08858250000620RP
0702-034-000
GUDID
0702034000
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 SURGICAL SMOKE EVACUATION SYSTEMS.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (23, all answered No)