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V8 Immunodisplacement Kit

FDA UDI

Class II (US FDA UDI)

by Helena Laboratories, Corp.

Identity

Trade Name
V8 Immunodisplacement Kit FDA UDI
Generic Name
Protein electrophoresis IVD, reagent FDA UDI
Model / Reference
1803 FDA UDI

Identifiers

Primary DI / UDI-DI
M52518030 FDA UDI
510(k) Number
K111369 FDA UDI
FDA Product Code
CFF FDA UDI
GMDN Term
Protein electrophoresis IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 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

No

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

No

FDA UDI

Category: Protein electrophoresis IVD, reagent

V8 Immunodisplacement Kit by Helena Laboratories, Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Protein electrophoresis IVD, reagent.

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 3d0f8733-7d23-4643-a015-6bc290424795 34 fields · synced Jun 9, 2026