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Retinol binding Protein (RBP)/RBP4 ELISA

FDA UDI

Class I (US FDA UDI)

by DRG Instruments Gesellschaft mit beschränkter Haftung

Identity

Trade Name
Retinol binding Protein (RBP)/RBP4 ELISA FDA UDI
Generic Name
Retinol binding protein IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
This assay is an enzyme immunoassay intended for the quantitative determination of free retinol-binding protein RBP/RBP4 as well as RBP4 complexed with transthyretin in plasma, serum and urine FDA UDI
Model / Reference
EIA-4391 FDA UDI
Description
This assay is an enzyme immunoassay intended for the quantitative determination of free retinol-binding protein RBP/RBP4 as well as RBP4 complexed with transthyretin in plasma, serum and urine FDA UDI

Identifiers

Catalog Number
EIA-4391 FDA UDI
Primary DI / UDI-DI
04048474043914 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

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

Yes

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

Yes

FDA UDI

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

Retinol binding Protein (RBP)/RBP4 ELISA by DRG Instruments Gesellschaft mit beschränkter Haftung — Class I — FDA UDI — listed in FDA GUDID

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

Sources (1)

  • FDA UDI 087ea640-8668-46e6-a2c6-d6ecfb1a3506 36 fields · synced Jun 8, 2026