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Lactoferrin ELISA

FDA UDI

Class I (US FDA UDI)

by Immundiagnostik, Inc.

Identity

Trade Name
Lactoferrin ELISA FDA UDI
Generic Name
Lactoferrin IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
K 6870.20.US FDA UDI

Identifiers

Primary DI / UDI-DI
04050598010413 FDA UDI
FDA Product Code
DEG FDA UDI
GMDN Term
Lactoferrin IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.5570 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lactoferrin IVD, kit, enzyme immunoassay (EIA)

Lactoferrin ELISA by Immundiagnostik, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lactoferrin 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 9de65a88-be63-4fed-902f-23de513078ea 33 fields · synced May 30, 2026