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Klassic ONE Knee PS-Post Auxiliary Instrumentation Tray

FDA UDI

Class I (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name
Klassic ONE Knee PS-Post Auxiliary Instrumentation Tray FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Knee PS-Post Auxiliary Instrumentation Tray FDA UDI
Model / Reference
2412.00.000 FDA UDI
Description
Knee PS-Post Auxiliary Instrumentation Tray FDA UDI

Identifiers

Primary DI / UDI-DI
00819251027861 FDA UDI
FDA Product Code
OJH FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Klassic ONE Knee PS-Post Auxiliary Instrumentation Tray by Total Joint Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dbdf1d3e-278d-4b42-a442-f0ed68d4d7bd 35 fields · synced May 30, 2026