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PyloPlus+ Rapid Urease Test

FDA UDI

Class I (US FDA UDI)

by Arj Medical, Inc.

Identity

Trade Name
PyloPlus+ Rapid Urease Test FDA UDI
Generic Name
Helicobacter pylori urease IVD, kit, chromogenic FDA UDI
Model / Reference
PYLO-50 FDA UDI

Identifiers

Primary DI / UDI-DI
00860001810394 FDA UDI
510(k) Number
K052708 FDA UDI
FDA Product Code
LYR FDA UDI
GMDN Term
Helicobacter pylori urease IVD, kit, chromogenic 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 urease IVD, kit, chromogenic

PyloPlus+ Rapid Urease Test by Arj Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Helicobacter pylori urease IVD, kit, chromogenic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arj Medical, Inc.

Sources (1)

  • FDA UDI 826a77a0-06d3-4235-ad6c-b03e5047e1ef 33 fields · synced Jun 8, 2026