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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Blood glucose/blood pressure monitoring system, home-use FDA UDI
Device Name
METER,GLUCOSE,EVENCARE PROVIEW,PROF.USE FDA UDI
Model / Reference
MPH4540 FDA UDI
Description
METER,GLUCOSE,EVENCARE PROVIEW,PROF.USE FDA UDI

Identifiers

Catalog Number
MPH4540 FDA UDI
Primary DI / UDI-DI
10888277409163 FDA UDI
510(k) Number
K111456 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Blood glucose/blood pressure monitoring system, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood glucose/blood pressure monitoring system, home-use

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

Similar devices

Also classified as Blood glucose/blood pressure monitoring system, home-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a2b95084-7004-419d-bcc3-ad2819fc0a10 36 fields · synced Jun 8, 2026