Mdf®

FDA UDI

Class II (US FDA UDI)

by MDF Instruments Medifriend Inc.

Identity

Trade Name: MDF® FDA UDI
Generic Name: Blood pressure cuff, reusable FDA UDI
Device Name: Blood Pressure Cuff, Large Adult D-Ring, Single Tube, MDF16 FDA UDI
Model / Reference: MDF2080461D16 FDA UDI
Description: Blood Pressure Cuff, Large Adult D-Ring, Single Tube, MDF16 FDA UDI

Identifiers

Primary DI / UDI-DI: 06940211634363 FDA UDI
FDA Product Code: DXQ FDA UDI
GMDN Term: Blood pressure cuff, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1120 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

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Blood pressure cuff, reusable

Mdf® by MDF Instruments Medifriend Inc. — 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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Unimed — Unimed Medical Supplies, Inc. · Class II
Orbit-K — SUNTECH MEDICAL, INC. · Class II
Disposable Cuff — SUNTECH MEDICAL, 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
Sklar® — Sklar Corporation · 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: MDF Instruments Medifriend Inc.

Sources (1)

FDA UDI 28b8fdf4-1d7e-4e90-9495-6f3bf6e7aa39 33 fields · synced May 31, 2026