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Anti-Sm ELISA

FDA UDI

Class II (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
Anti-Sm ELISA FDA UDI
Generic Name
Multiple extractable nuclear antigen (ENA) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Anti-Sm ELISA is a test system for the quantitative measurement of IgG class autoantibodies against Sm in human serum or plasma. FDA UDI
Model / Reference
EIA-3577 FDA UDI
Description
Anti-Sm ELISA is a test system for the quantitative measurement of IgG class autoantibodies against Sm in human serum or plasma. FDA UDI

Identifiers

Catalog Number
EIA-3577 FDA UDI
Primary DI / UDI-DI
00840239035776 FDA UDI
510(k) Number
K962062 FDA UDI
FDA Product Code
LJM FDA UDI
GMDN Term
Multiple extractable nuclear antigen (ENA) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple extractable nuclear antigen (ENA) IVD, kit, enzyme immunoassay (EIA)

Anti-Sm ELISA by DRG International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple extractable nuclear antigen (ENA) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 50626682-6dee-4dca-80da-81a67c4685ac 37 fields · synced May 30, 2026