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Light Diagnostics ™ Rabies Negative Control Concentrate

FDA UDI

Class II (US FDA UDI)

by Emd Millipore Corporation

Identity

Trade Name
Light Diagnostics ™ Rabies Negative Control Concentrate FDA UDI
Generic Name
Rabies virus antigen IVD, antibody FDA UDI
Device Name
Rabies Negative Control Concentrate FDA UDI
Model / Reference
5102 FDA UDI
Description
Rabies Negative Control Concentrate FDA UDI

Identifiers

Catalog Number
5102 FDA UDI
Primary DI / UDI-DI
04053252585999 FDA UDI
FDA Product Code
GOI FDA UDI
GMDN Term
Rabies virus antigen IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3460 FDA UDI
Commercial Distribution
Not 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

Light Diagnostics ™ Rabies Negative Control Concentrate by Emd Millipore Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d315b94-0b5d-4f6a-87b0-096e66051a1f 37 fields · synced May 30, 2026