← Back to catalogue

Abx Pentra Aso Cp

FDA UDI

Class I (US FDA UDI)

by Horiba Abx

Identity

Trade Name
ABX PENTRA ASO CP FDA UDI
Generic Name
Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
1220001980 FDA UDI

Identifiers

Primary DI / UDI-DI
03610230005811 FDA UDI
FDA Product Code
GTQ FDA UDI
GMDN Term
Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3720 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: Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry

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

Similar devices

Also classified as Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Horiba Abx

Sources (1)

  • FDA UDI f2841bd7-4f05-4f50-b6de-4bf5f203ca7c 32 fields · synced Jun 1, 2026