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B155M Patient Monitor

by GE Medical Systems Information Technologies, Inc. 2 variants

Ref 6160000-005Model B105P B125P B105M B125M B155M

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

Not listed

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

6 ongoing

This device is named in the recall

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K242562↗

+1 more

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, FDA 510(k), GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k) 510(k) NumberK242562 Date9 Jul 2025IssuedStatusActive
United StatesGUDID listing GUDID Number00840682146791 UDI-DI Date12 Apr 2022ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number8406821BUG00102GM Basic UDI-DI 00840682146791UDI-DIDate30 Mar 2022RegisteredStatusActive

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

6 recalls · 6 ongoing · FDA

    • Ongoing Z-0455-2026 FDA Class II initiated 26 Sep 2025

    Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

  • 5 recalls, same reason

    • Ongoing Z-0730-2023 FDA Class II initiated 16 Nov 2022
    • Ongoing Z-0732-2023 FDA Class II initiated 16 Nov 2022
    • Ongoing Z-0731-2023 FDA Class II initiated 16 Nov 2022
    • Ongoing Z-0733-2023 FDA Class II initiated 16 Nov 2022
    • Ongoing Z-0729-2023 FDA Class II initiated 16 Nov 2022

    GE Healthcare has become aware that if certain B1x5P / B1x5M patient monitors use "mmHg" or "kPa" as the unit for CO2 measurement, the displayed value for CO2 measurement can be inaccurate when used in a location that is not at or near sea level.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • United States FDA 510(k) Active
  • European Union CE/MDR Active

Specification

EUDAMED · 510(k) · GUDID

Generic Name
General-purpose multi-parameter bedside monitor
Device Name
B105P B125P B105M B125M B155M Patient Monitors
Model / Ref / Catalog
B105P B125P B105M B125M B155M, 6160000-005, B155 VSP3.0 Patient Monitor
Description
B155M ATO MODEL
Primary DI / UDI-DI
00840682146791
Basic UDI-DI
8406821BUG00102GM
510(k) Number
FDA Product Code
DRT, KOI, DSJ, DXN, OMC, DSI, DSK, MHX, NHO, ORT, CBQ, GWQ, OLW, DQA, CBS, CCL, DQK, CCK, KRB, MLD, OLT, DPZ, BZQ, FLL, CBR, NHQ, NHP
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
870.2300, 868.2775, 870.1100, 870.1130, 882.1400, 870.1025, 870.1110, 868.1500, 870.2700, 868.1620, 868.1720, 870.1425, 868.1400, 870.1915, 870.2710, 868.2375, 880.2910, 868.1700
EU market of registration
France
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
B105P B125P B105M B125M B155M
6160000-005
GUDID
B155 VSP3.0 Patient Monitor
Device ClassEUDAMED
Class IIb
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000017529
Authorised representative
GE Medical Systems SCS FR-AR-000000344

Other devices from GE Medical Systems Information Technologies, Inc.

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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