← Back to catalogue

Vp 1 + Vp 2

FDA UDI

Class I (US FDA UDI)

by Biomerieux , Inc.

Identity

Trade Name
VP 1 + VP 2 FDA UDI
Generic Name
Multiple Enterobacteriaceae species culture isolate identification IVD, reagent FDA UDI
Device Name
VP1 VP2 are reagents associated to API 20 E™ (20 100/20 160), RapiD 20 E™ (20 701), API® Staph (20 500), API® 20 Strep (20 600) FDA UDI
Model / Reference
70422 FDA UDI
Description
VP1 VP2 are reagents associated to API 20 E™ (20 100/20 160), RapiD 20 E™ (20 701), API® Staph (20 500), API® 20 Strep (20 600) FDA UDI

Identifiers

Primary DI / UDI-DI
03573026099626 FDA UDI
FDA Product Code
JTO FDA UDI
GMDN Term
Multiple Enterobacteriaceae species culture isolate identification IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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

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 Enterobacteriaceae species culture isolate identification IVD, reagent

Vp 1 + Vp 2 by Biomerieux , Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple Enterobacteriaceae species culture isolate identification IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biomerieux , Inc.

Sources (1)

  • FDA UDI c0636143-81b8-4164-91f9-aa32221ba914 34 fields · synced May 30, 2026