← Back to catalogue

FLEX Mono Mo A-Hu CDX2 Cl DAK-CDX2 RTU

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
FLEX Mono Mo A-Hu CDX2 Cl DAK-CDX2 RTU FDA UDI
Generic Name
Homeobox protein CDX-2 IVD, antibody FDA UDI
Device Name
FLEX Monoclonal Mouse Anti-Human CDX2 Clone DAK-CDX2 Ready-to-Use (Dako Autostainer/ Autostainer Plus) FDA UDI
Model / Reference
IS080 FDA UDI
Description
FLEX Monoclonal Mouse Anti-Human CDX2 Clone DAK-CDX2 Ready-to-Use (Dako Autostainer/ Autostainer Plus) FDA UDI

Identifiers

Primary DI / UDI-DI
05700571101407 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Homeobox protein CDX-2 IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

FLEX Mono Mo A-Hu CDX2 Cl DAK-CDX2 RTU by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI bfaa6745-6aae-43df-b95f-6a3d9378f378 37 fields · synced Jun 8, 2026