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Lysozyme (stool) ELISA

FDA UDI

Class I (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
Lysozyme (stool) ELISA FDA UDI
Generic Name
Lysozyme (muramidase) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
This assay is an enzyme immunoassay intended for the quantitative determination of lysozyme in stool. FDA UDI
Model / Reference
EIA-6100 FDA UDI
Description
This assay is an enzyme immunoassay intended for the quantitative determination of lysozyme in stool. FDA UDI

Identifiers

Catalog Number
EIA-6100 FDA UDI
Primary DI / UDI-DI
00840239061003 FDA UDI
FDA Product Code
JMQ FDA UDI
GMDN Term
Lysozyme (muramidase) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1490 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Lysozyme (stool) ELISA by DRG International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb277074-4f39-41dd-8efe-a157fbfa4a8b 37 fields · synced May 30, 2026