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FLEX Poly Rb A-Hu CD3 RTU (Dako Omnis)

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Singapore Pte Ltd

Identity

Trade Name
FLEX Poly Rb A-Hu CD3 RTU (Dako Omnis) FDA UDI
Generic Name
CD3 cell marker IVD, antibody FDA UDI
Device Name
FLEX Polyclonal Rabbit Anti-Human CD3 Ready-to-Use (Dako Omnis) FDA UDI
Model / Reference
GA503 FDA UDI
Description
FLEX Polyclonal Rabbit Anti-Human CD3 Ready-to-Use (Dako Omnis) FDA UDI

Identifiers

Primary DI / UDI-DI
05700572033059 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
CD3 cell marker IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Commercial Distribution
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

Dimensions & Sizes

Size
Total Volume — 12 Milliliter FDA UDI

Category: CD3 cell marker IVD, antibody

FLEX Poly Rb A-Hu CD3 RTU (Dako Omnis) by Agilent Technologies Singapore Pte Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CD3 cell marker IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16645932-d767-4812-8b39-4967a464059b 36 fields · synced Jun 6, 2026