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Dako

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
Dako FDA UDI
Generic Name
Gross cystic disease fluid protein-15 IVD, antibody FDA UDI
Device Name
FLEX Monoclonal Mouse Anti-Human Gross Cystic Disease Fluid Protein-15 Clone 23A3 Ready-to-Use (Dako Autostainer/ Autostainer Plus) FDA UDI
Model / Reference
IS077 FDA UDI
Description
FLEX Monoclonal Mouse Anti-Human Gross Cystic Disease Fluid Protein-15 Clone 23A3 Ready-to-Use (Dako Autostainer/ Autostainer Plus) FDA UDI

Identifiers

Primary DI / UDI-DI
05700571101391 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Gross cystic disease fluid protein-15 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

Dako 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 e85065c4-62bb-4469-bb92-41cd85d46fd0 37 fields · synced May 30, 2026