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BeneVision N19 Patient Monitor

by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Ref BeneVision N19Model BeneVision N22/BeneVision N22 OR/BeneVision N22 ICU/BeneVision N19/BeneVision N19 OR/BeneVision N19 ICU/ BeneVision M22/BeneVision M22C/BeneVision M19/BeneVision M19C

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

CE MDR

Valid until

Not listed

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

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/MDR EUDAMED Number69449040AB0100002238 Basic UDI-DI 06944904095608UDI-DIDate7 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06944904095608 UDI-DI Date24 Jan 2025ListedStatusListed 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.

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  • Withdrawn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
Patient monitor EUDAMED
BeneVision N19 Patient Monitor GUDID
Generic Name
General-purpose multi-parameter bedside monitor
Model / Reference
BeneVision N19, BeneVision N22/BeneVision N22 OR/BeneVision N22 ICU/BeneVision N19/BeneVision N19 OR/BeneVision N19 ICU/ BeneVision M22/BeneVision M22C/BeneVision M19/BeneVision M19C
Primary DI / UDI-DI
06944904095608
Basic UDI-DI
69449040AB0100002238
FDA Product Code
MHX
EMDN Code
Z1203020201 Multi–parameter patient bedside monitors
GMDN Term
General-purpose multi-parameter bedside monitor
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
870.1025
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class II

Related devices

Category: General-purpose multi-parameter bedside monitor

Other devices from Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

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Properties

  • Measuring Function
  • Serial Number
  • Manufacturing Date

Other properties (21)

  • 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
  • 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
  • Expiration Date: No