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FLEX Mono Mo A-Hu CD1a Cl 010 RTU

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
FLEX Mono Mo A-Hu CD1a Cl 010 RTU FDA UDI
Generic Name
CD1a cell marker IVD, antibody FDA UDI
Device Name
FLEX Monoclonal Mouse Anti-Human CD1a Clone 010 Ready-to-Use (Dako Autostainer/ Autostainer Plus) FDA UDI
Model / Reference
IS069 FDA UDI
Description
FLEX Monoclonal Mouse Anti-Human CD1a Clone 010 Ready-to-Use (Dako Autostainer/ Autostainer Plus) FDA UDI

Identifiers

Primary DI / UDI-DI
05700571101346 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
CD1a cell marker 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 CD1a Cl 010 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

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Manufacturer

Sources (1)

  • FDA UDI c4fa1158-10b2-403d-837e-160199a76803 37 fields · synced Jun 1, 2026