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NA enspire 3000 Maxflow Connector

by Steris Corporation 28 variants

Ref ENLCS632Model Maxflow Connectors

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 24 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995CMEN3000MXFLCNVY Basic UDI-DI 00724995229009UDI-DIDate23 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995229009 UDI-DI Date3 Jun 2024ListedStatusListed 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 24 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  • Withdrawn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

Generic Name
Luminal device flushing tubing set, reusable
Device Name
Maxflow Connectors
Model / Ref / Catalog
Maxflow Connectors, ENLCS632, enspire 3000 Maxflow Connector
Primary DI / UDI-DI
00724995229009
Basic UDI-DI
0724995CMEN3000MXFLCNVY
510(k) Number
FDA Product Code
FEB
EMDN Code
S9002 Devices for sterilisation with peracetic acid (excluding cat. d - z)
GMDN Term
Luminal device flushing tubing set, reusable
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
876.1500
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Maxflow Connectors
ENLCS632
GUDID
enspire 3000 Maxflow Connector
Device ClassEUDAMED
Class I
GUDID
Class II

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Manufacturing Date

Other properties (23)

  • Sterile: No
  • Single Use: 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
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No