Unimed

FDA UDI

Class II (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name: Unimed FDA UDI
Generic Name: Blood pressure cuff, single-use FDA UDI
Device Name: Disposable NIBP Cuff/Textile/Double tube/Big Adult/with BP12-P connector/Sage Services GROUP FDA UDI
Model / Reference: DC720D-C12 FDA UDI
Description: Disposable NIBP Cuff/Textile/Double tube/Big Adult/with BP12-P connector/Sage Services GROUP FDA UDI

Identifiers

Primary DI / UDI-DI: 06945664874816 FDA UDI
FDA Product Code: DXQ FDA UDI
GMDN Term: Blood pressure cuff, single-use 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

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood pressure cuff, single-use

Unimed by Unimed Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Orantech — Orantech Inc. · Class II
Softcheck — STATCORP MEDICAL · 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: Unimed Medical Supplies, Inc.

Sources (1)

FDA UDI ef51de3e-1f5b-474e-a139-ef3b8fd61718 33 fields · synced Jun 8, 2026