← Back to catalogue

Small Adult NBP Cuffs (10)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 989803182531

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
Small Adult NBP Cuffs (10) EUDAMED
MR Patient Care Small Adult NBP Cuffs (10) FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Non-Invasive Blood Pressure Cuffs EUDAMED
NiBP Cuff, Single Lumen,Small Adult,Disp. Box of 10 FDA UDI
Model / Reference
989803182531 EUDAMED
Small Adult NBP Cuffs (10) FDA UDI
Description
NiBP Cuff, Single Lumen,Small Adult,Disp. Box of 10 FDA UDI

Identifiers

Catalog Number
989803182531 FDA UDI
Primary DI / UDI-DI
10884838120829 EUDAMEDFDA UDI
Basic UDI-DI
0884838BM1073M4 EUDAMED
Unit of Use DI
00884838120822 EUDAMED
FDA Product Code
MWI FDA UDI
EMDN Code
Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES 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

Yes

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

Category: General-purpose multi-parameter bedside monitor

Small Adult NBP Cuffs (10) by Philips Medizin Systeme Böblingen GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

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

EUDAMED SRN
DE-MF-000006026

Sources (2)

  • EUDAMED d4594fe8-d56e-4237-b639-fd9e78d2684c 61 fields · synced Jul 16, 2026
  • FDA UDI 02805f15-2bfa-4387-849d-626b94c3292d 35 fields · synced May 30, 2026