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E. coli reference strain O9

FDA UDI

Class I (US FDA UDI)

by Ssi Diagnostica A/S

Identity

Trade Name
E. coli reference strain O9 FDA UDI
Generic Name
Escherichia coli antigen IVD, control FDA UDI
Device Name
Reference strain FDA UDI
Model / Reference
81842 FDA UDI
Description
Reference strain FDA UDI

Identifiers

Catalog Number
81842 FDA UDI
Primary DI / UDI-DI
05713106818428 FDA UDI
FDA Product Code
GMZ FDA UDI
GMDN Term
Escherichia coli antigen IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3255 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: Escherichia coli antigen IVD, control

E. coli reference strain O9 by Ssi Diagnostica A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Escherichia coli antigen IVD, control.

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 1e7ce3f5-d5ec-4e9e-9697-213971d87d0e 36 fields · synced Jun 1, 2026