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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Helicobacter pylori antigen IVD, control FDA UDI
Device Name
TEST,H.PYLORI,CASS,25 TEST FDA UDI
Model / Reference
MPH42025HP FDA UDI
Description
TEST,H.PYLORI,CASS,25 TEST FDA UDI

Identifiers

Catalog Number
MPH42025HP FDA UDI
Primary DI / UDI-DI
20888277717777 FDA UDI
FDA Product Code
LYR FDA UDI
GMDN Term
Helicobacter pylori antigen IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3110 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Helicobacter pylori antigen IVD, control

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

Similar devices

Also classified as Helicobacter pylori antigen IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a63f148b-18d9-4507-88fc-45848818aa3a 36 fields · synced May 30, 2026