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MedMira Rapid H. Pylori Antibody Test

FDA UDI

Class I (US FDA UDI)

by MedMira Laboratories Inc

Identity

Trade Name
MedMira Rapid H. Pylori Antibody Test FDA UDI
Generic Name
Helicobacter pylori antigen IVD, kit, rapid ICT, clinical FDA UDI
Device Name
The MedMira Rapid H. Pylori Antibody Test is a rapid flow through test developed and manufactured by MedMira Laboratories Inc. FDA UDI
Model / Reference
815311003820 FDA UDI
Description
The MedMira Rapid H. Pylori Antibody Test is a rapid flow through test developed and manufactured by MedMira Laboratories Inc. FDA UDI

Identifiers

Primary DI / UDI-DI
00628451188278 FDA UDI
510(k) Number
K002023 FDA UDI
FDA Product Code
LYR FDA UDI
GMDN Term
Helicobacter pylori antigen IVD, kit, rapid ICT, clinical 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

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

No

FDA UDI

Category: Helicobacter pylori antigen IVD, kit, rapid ICT, clinical

MedMira Rapid H. Pylori Antibody Test by MedMira Laboratories Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Helicobacter pylori antigen IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4a3c692c-c0d1-401b-8115-7899ede9c437 35 fields · synced May 30, 2026