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Optilite Beta 2 Microglobulin Urine Kit

FDA UDI

Class II (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
Optilite Beta 2 Microglobulin Urine Kit FDA UDI
Generic Name
Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
LK043.L.OPT.A FDA UDI

Identifiers

Primary DI / UDI-DI
05051700017688 FDA UDI
510(k) Number
K122066 FDA UDI
FDA Product Code
JZG FDA UDI
GMDN Term
Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5630 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

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: Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry

Optilite Beta 2 Microglobulin Urine Kit by The Binding Site Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Beta-2-microglobulin IVD, kit, nephelometry/turbidimetry.

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 c93bd8a2-beb3-46ee-9cb5-74ad4e0f14dd 35 fields · synced May 30, 2026