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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Manual-inflation electronic sphygmomanometer, portable FDA UDI
Device Name
MONITOR,BP,SEMI AUTO,DIGITAL,ADULT FDA UDI
Model / Reference
MDS3002 FDA UDI
Description
MONITOR,BP,SEMI AUTO,DIGITAL,ADULT FDA UDI

Identifiers

Catalog Number
MDS3002 FDA UDI
Primary DI / UDI-DI
00080196525167 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Manual-inflation electronic sphygmomanometer, portable 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

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

Yes

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

No

FDA UDI

Category: Manual-inflation electronic sphygmomanometer, portable

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual-inflation electronic sphygmomanometer, portable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 39668461-f66f-4849-8604-1d3856b2195f 35 fields · synced May 30, 2026