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Salmonella Gruppe O:47 serum, 3 mL

FDA UDI

Class II (US FDA UDI)

by Ssi Diagnostica A/S

Identity

Trade Name
Salmonella Gruppe O:47 serum, 3 mL FDA UDI
Generic Name
Multiple Salmonella species culture isolate antigen IVD, antibody FDA UDI
Device Name
Rabbit antiserum, Ready to use FDA UDI
Model / Reference
40245 FDA UDI
Description
Rabbit antiserum, Ready to use FDA UDI

Identifiers

Catalog Number
40245 FDA UDI
Primary DI / UDI-DI
05713106402450 FDA UDI
FDA Product Code
GRM FDA UDI
GMDN Term
Multiple Salmonella species culture isolate antigen IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3550 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

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: Multiple Salmonella species culture isolate antigen IVD, antibody

Salmonella Gruppe O:47 serum, 3 mL by Ssi Diagnostica A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple Salmonella species culture isolate antigen IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ssi Diagnostica A/S

Sources (1)

  • FDA UDI 074e0a49-ac8b-452d-8887-b087f03813f5 36 fields · synced Jun 6, 2026