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Poly Rb A-Hu Fibrinogen/FITC

FDA UDI

Class II (US FDA UDI)

by Agilent Technologies Singapore Pte Ltd

Identity

Trade Name
Poly Rb A-Hu Fibrinogen/FITC FDA UDI
Generic Name
Fibrinogen (Factor I) assay IVD, antibody FDA UDI
Device Name
Polyclonal Rabbit Anti-Human Fibrinogen/FITC FDA UDI
Model / Reference
F0111 FDA UDI
Description
Polyclonal Rabbit Anti-Human Fibrinogen/FITC FDA UDI

Identifiers

Primary DI / UDI-DI
05700572002376 FDA UDI
FDA Product Code
DAX FDA UDI
GMDN Term
Fibrinogen (Factor I) assay IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7340 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 — 2 Milliliter FDA UDI

Category: Fibrinogen (Factor I) assay IVD, antibody

Poly Rb A-Hu Fibrinogen/FITC by Agilent Technologies Singapore Pte Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibrinogen (Factor I) assay IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aed0f1dd-026c-48d1-9eab-6ef5f7423014 36 fields · synced Jun 8, 2026