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Latex Calibrators

FDA UDI

Class I (US FDA UDI)

by Alifax Srl

Identity

Trade Name
LATEX CALIBRATORS FDA UDI
Generic Name
Erythrocyte sedimentation rate (ESR) IVD, calibrator FDA UDI
Model / Reference
LATEX CALIBRATORS FDA UDI

Identifiers

Catalog Number
SI 305.400-A FDA UDI
Primary DI / UDI-DI
08056040141236 FDA UDI
FDA Product Code
GKB FDA UDI
GMDN Term
Erythrocyte sedimentation rate (ESR) IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.5800 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

Category: Erythrocyte sedimentation rate (ESR) IVD, calibrator

Latex Calibrators by Alifax Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Erythrocyte sedimentation rate (ESR) IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alifax Srl

Sources (1)

  • FDA UDI 5f475f09-22ec-4c99-926a-ec52b23dba34 34 fields · synced May 30, 2026