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SSA (Ro) ELISA

FDA UDI

Class II (US FDA UDI)

by DRG Instruments Gesellschaft mit beschränkter Haftung

Identity

Trade Name
SSA (Ro) ELISA FDA UDI
Generic Name
Multiple extractable nuclear antigen (ENA) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The DRG ELISA SSA (Ro) ELISA is designed to detect IgG class antibodies to SSA in human sera. FDA UDI
Model / Reference
EIA-2782 FDA UDI
Description
The DRG ELISA SSA (Ro) ELISA is designed to detect IgG class antibodies to SSA in human sera. FDA UDI

Identifiers

Catalog Number
EIA-2782 FDA UDI
Primary DI / UDI-DI
04048474027822 FDA UDI
510(k) Number
K941409 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)

SSA (Ro) ELISA by DRG Instruments Gesellschaft mit beschränkter Haftung — 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).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c3f8e67-47c0-4444-8291-12d744a7b924 37 fields · synced May 30, 2026