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Hevylite® Human IgG Lambda Kit for use on the Siemens BN™II

FDA UDI

by The Binding Site Group

Identity

Trade Name
Hevylite® Human IgG Lambda Kit for use on the Siemens BN™II FDA UDI
Generic Name
Total immunoglobulin G (IgG total) IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
NK622.T FDA UDI

Identifiers

Primary DI / UDI-DI
05051700012461 FDA UDI
GMDN Term
Total immunoglobulin G (IgG total) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

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

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

Category: Total immunoglobulin G (IgG total) IVD, kit, nephelometry/turbidimetry

Hevylite® Human IgG Lambda Kit for use on the Siemens BN™II by The Binding Site Group — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total immunoglobulin G (IgG total) IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9f550f3a-14a8-4413-97c0-81208cb58097 34 fields · synced May 30, 2026