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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 blood pressure cuff/non-woven/double tubing/Adult/with BP08 connector /pluscare FDA UDI
Model / Reference
PN1740D-C0808-05 FDA UDI
Description
Disposable blood pressure cuff/non-woven/double tubing/Adult/with BP08 connector /pluscare FDA UDI

Identifiers

Primary DI / UDI-DI
06945664877992 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

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

Similar devices

Also classified as Blood pressure cuff, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a94a8cef-e251-4179-8b8a-a5ba0d4f795d 33 fields · synced May 30, 2026