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SPIFE Vis Cholesterol Kit

FDA UDI

Class I (US FDA UDI)

by Helena Laboratories, Corp.

Identity

Trade Name
SPIFE Vis Cholesterol Kit FDA UDI
Generic Name
Protein electrophoresis IVD, kit, electrophoresis FDA UDI
Model / Reference
551919 FDA UDI

Identifiers

Primary DI / UDI-DI
M5255519190 FDA UDI
510(k) Number
K000603 FDA UDI
FDA Product Code
JHO FDA UDI
GMDN Term
Protein electrophoresis IVD, kit, electrophoresis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1475 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, kit, electrophoresis

SPIFE Vis Cholesterol Kit by Helena Laboratories, Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Protein electrophoresis IVD, kit, electrophoresis.

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 8699326f-1203-4917-8295-4c1d9e57470d 34 fields · synced Jun 9, 2026