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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, reusable FDA UDI
Device Name
Reusable NIBP Cuff with inflation bag Single tube and connector Adult Long Range 27.5-36.5cm FDA UDI
Model / Reference
GB2286ND-C48 FDA UDI
Description
Reusable NIBP Cuff with inflation bag Single tube and connector Adult Long Range 27.5-36.5cm FDA UDI

Identifiers

Primary DI / UDI-DI
06936735470389 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood pressure cuff, reusable

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, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32b9fed0-2af1-47b5-b785-5e9047cbd5b1 33 fields · synced May 29, 2026