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OxyPRAS Plus KVL plate

FDA UDI

Class I (US FDA UDI)

by Oxyrase, Inc.

Identity

Trade Name
OxyPRAS Plus KVL plate FDA UDI
Generic Name
Differential/selective agar culture medium IVD FDA UDI
Device Name
Culture Media, Selective and Non-Differential FDA UDI
Model / Reference
P-KVL-BA FDA UDI
Description
Culture Media, Selective and Non-Differential FDA UDI

Identifiers

Catalog Number
P-KVL-BA FDA UDI
Primary DI / UDI-DI
00850056467049 FDA UDI
FDA Product Code
JSJ FDA UDI
GMDN Term
Differential/selective agar culture medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 24 Gram FDA UDI

Category: Differential/selective agar culture medium IVD

OxyPRAS Plus KVL plate by Oxyrase, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Differential/selective agar culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oxyrase, Inc.

Sources (1)

  • FDA UDI 7fe16e02-0266-4820-9428-36d88ff110f8 37 fields · synced May 30, 2026