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N Antiserum to Human RBP

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
N Antiserum to Human RBP FDA UDI
Generic Name
Retinol binding protein IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Quantitative determination of retinol-binding protein in human serum and plasma on BN Systems FDA UDI
Model / Reference
10446494 FDA UDI
Description
Quantitative determination of retinol-binding protein in human serum and plasma on BN Systems FDA UDI

Identifiers

Catalog Number
OUVO09 FDA UDI
Primary DI / UDI-DI
00842768011856 FDA UDI
FDA Product Code
CZS FDA UDI
GMDN Term
Retinol binding protein IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.5765 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Retinol binding protein IVD, kit, nephelometry/turbidimetry

N Antiserum to Human RBP by Siemens Healthcare Diagnostics Products Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Retinol binding protein IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare Diagnostics Products Ltd

Sources (1)

  • FDA UDI c183bbed-41c1-4407-8e81-002e0f942943 36 fields · synced May 30, 2026