← Back to catalogue

Small Adult NBP Cuff

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 989803182631

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
Small Adult NBP Cuff EUDAMED
MR Patient Care Small Adult NBP Cuff FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Non-Invasive Blood Pressure Cuffs EUDAMED
NiBP Cuff, Single Lumen, Small Adult FDA UDI
Model / Reference
989803182631 EUDAMED
Small Adult NBP Cuff FDA UDI
Description
NiBP Cuff, Single Lumen, Small Adult FDA UDI

Identifiers

Catalog Number
989803182631 FDA UDI
Primary DI / UDI-DI
00884838120914 EUDAMEDFDA UDI
Basic UDI-DI
0884838BM1073M4 EUDAMED
Direct Marketing DI
00884838120914 EUDAMED
FDA Product Code
MWI FDA UDI
EMDN Code
Z1203020299 MULTI–PARAMETER MONITORS - OTHER EUDAMED
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Small Adult NBP Cuff by Philips Medizin Systeme Böblingen GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Philips Medizin Systeme Böblingen GmbH
EUDAMED SRN
DE-MF-000006026

Sources (2)

  • EUDAMED 4b0ff058-8ea9-4bb0-ae3b-a7154f36e375 61 fields · synced Jul 25, 2026
  • FDA UDI 1108abc3-378d-408e-a344-462495f152a0 35 fields · synced May 26, 2026