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Human Immunoglobulin D BINDARID™ Radial Immunodiffusion Kit

FDA UDI

Class II (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
Human Immunoglobulin D BINDARID™ Radial Immunodiffusion Kit FDA UDI
Generic Name
Total immunoglobulin D (IgD total) IVD, antibody FDA UDI
Model / Reference
RN013.3 FDA UDI

Identifiers

Primary DI / UDI-DI
05051700010474 FDA UDI
510(k) Number
K913671 FDA UDI
FDA Product Code
CZJ FDA UDI
GMDN Term
Total immunoglobulin D (IgD total) IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 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: Total immunoglobulin D (IgD total) IVD, antibody

Human Immunoglobulin D BINDARID™ Radial Immunodiffusion Kit by The Binding Site Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total immunoglobulin D (IgD total) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e3216ef-4eda-46a4-805f-4891dc46da74 35 fields · synced May 30, 2026