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Immco Diagnostics

FDA UDI

by Immco Diagnostics, Inc.

Identity

Trade Name
IMMCO DIAGNOSTICS FDA UDI
Generic Name
SSA/Ro antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
SS-A (Ro) 52kD and 60kD Antibody ELISA FDA UDI
Model / Reference
5128 FDA UDI
Description
SS-A (Ro) 52kD and 60kD Antibody ELISA FDA UDI

Identifiers

Catalog Number
5128 FDA UDI
Primary DI / UDI-DI
00845714002250 FDA UDI
GMDN Term
SSA/Ro antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

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

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: SSA/Ro antibody (Sjogren's antibody) IVD, kit, enzyme immunoassay (EIA)

Immco Diagnostics by Immco Diagnostics, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as SSA/Ro antibody (Sjogren's antibody) 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 10644d29-0aad-4bbd-9b4a-867d0da1192e 37 fields · synced Sep 17, 2026