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Abx Pentra Urine Control L/H

FDA UDI

Class I (US FDA UDI)

by Horiba Abx

Identity

Trade Name
ABX PENTRA URINE CONTROL L/H FDA UDI
Generic Name
Multiple urine analyte IVD, control FDA UDI
Model / Reference
1220001674 FDA UDI

Identifiers

Primary DI / UDI-DI
03610230005248 FDA UDI
510(k) Number
K072115 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple urine analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple urine analyte IVD, control

Abx Pentra Urine Control L/H by Horiba Abx — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple urine analyte IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Horiba Abx

Sources (1)

  • FDA UDI 081ec8b8-356c-4c8b-940c-47d80589fac3 33 fields · synced Jun 1, 2026