MR Patient Care Infant NBP Cuff

FDA UDI

Class II (US FDA UDI)

by Philips DS North America LLC

Identity

Trade Name: MR Patient Care Infant NBP Cuff FDA UDI
Generic Name: Blood pressure cuff, reusable FDA UDI
Model / Reference: NiBP Cuff, Single Lumen, Infant FDA UDI

Identifiers

Catalog Number: 989803182611 FDA UDI
Primary DI / UDI-DI: 00884838034075 FDA UDI
FDA Product Code: DXN FDA UDI
GMDN Term: Blood pressure cuff, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1130 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Blood pressure cuff, reusable

MR Patient Care Infant NBP Cuff by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

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Disposable Cuff — SUNTECH MEDICAL, INC. · Class II
MDF® — MDF Instruments Medifriend Inc. · Class II
Disposable Cuff — SUNTECH MEDICAL, INC. · Class II
Extra Large Cuff Assembly for HEM-907XL — Omron Healthcare, Inc. · Class II
Welch Allyn, Inc. — Welch Allyn, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Philips DS North America LLC

Sources (1)

FDA UDI 483b24e1-2852-45af-bac7-ad07d142e04a 34 fields · synced Jun 8, 2026