← Back to catalogue

Gentle Care Cuff, Infant 1-Tube

EUDAMEDFDA UDI

Class I (EU MDR)

Ref M4572B

by Philips Medical Systems

Identity

Trade Name
GENTLE CARE CUFF, INFANT 1-TUBE EUDAMED
NIBP Cuffs FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
Easy Care Cuffs and Gentle Care Cuffs EUDAMED
Gentle Care Cuff, Infant, 1-tube (orange). Soft Single Patient. Circumference 10.0 - 15.0 cm. 10/box. FDA UDI
Model / Reference
M4572B EUDAMED
GENTLE CARE CUFF, INFANT 1-TUBE FDA UDI
Description
Gentle Care Cuff, Infant, 1-tube (orange). Soft Single Patient. Circumference 10.0 - 15.0 cm. 10/box. FDA UDI

Identifiers

Catalog Number
M4572B FDA UDI
Primary DI / UDI-DI
20884838009022 EUDAMEDFDA UDI
Basic UDI-DI
0884838BM339T4 EUDAMED
Unit of Use DI
00884838009028 EUDAMED
FDA Product Code
OED 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
870.1120 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
Not 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Gentle Care Cuff, Infant 1-Tube by Philips Medical Systems — 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

EUDAMED SRN
US-MF-000002321
Authorised Representative
Philips Medical Systems Nederland B.V. NL-AR-000001422

Sources (2)

  • EUDAMED 2f062f50-1e4c-4394-ade9-c375fffc1580 61 fields · synced Jul 30, 2026
  • FDA UDI 9a09e563-f8f9-4d90-b473-85a8a2cd5e12 37 fields · synced May 30, 2026