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Immunofixation (IFE) Kit

FDA UDI

Class II (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
Immunofixation (IFE) Kit FDA UDI
Generic Name
Protein electrophoresis IVD, kit, electrophoresis FDA UDI
Model / Reference
XK001 FDA UDI

Identifiers

Primary DI / UDI-DI
05051700011211 FDA UDI
FDA Product Code
CFF FDA UDI
GMDN Term
Protein electrophoresis IVD, kit, electrophoresis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Immunofixation (IFE) Kit by The Binding Site Group — Class II — 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 985d46e5-8859-434d-b7a4-ea5a47167317 35 fields · synced May 30, 2026