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Slxfa-Si

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
SLXFA-SI FDA UDI
Generic Name
Microplate reader IVD, automated/semi-automated FDA UDI
Device Name
Multi-Mode Microplate Reader FDA UDI
Model / Reference
SLXFA-SI FDA UDI
Description
Multi-Mode Microplate Reader FDA UDI

Identifiers

Primary DI / UDI-DI
05700574035419 FDA UDI
FDA Product Code
JJQ FDA UDI
GMDN Term
Microplate reader IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2300 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microplate reader IVD, automated/semi-automated

Slxfa-Si by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microplate reader IVD, automated/semi-automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agilent Technologies Inc.

Sources (1)

  • FDA UDI 534b4e0b-920a-4cbd-bd92-858a57d9f6e5 35 fields · synced Jun 1, 2026