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Abx Pentra Precitest Solution

FDA UDI

Class I (US FDA UDI)

by Horiba Abx

Identity

Trade Name
ABX PENTRA PRECITEST SOLUTION FDA UDI
Generic Name
Optical laboratory instrument performance standard calibrator/control IVD, single-use FDA UDI
Model / Reference
1300017438 FDA UDI

Identifiers

Primary DI / UDI-DI
03610230006771 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Optical laboratory instrument performance standard calibrator/control IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Optical laboratory instrument performance standard calibrator/control IVD, single-use

Abx Pentra Precitest Solution by Horiba Abx — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Optical laboratory instrument performance standard calibrator/control IVD, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Horiba Abx

Sources (1)

  • FDA UDI dcc1db57-06cd-4390-832e-c1a6a7955c10 32 fields · synced May 30, 2026