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KneeTools V5 Kit

FDA UDI

Class II (US FDA UDI)

by Pixee Medical

Identity

Trade Name
KneeTools V5 Kit FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Kit of reusable instruments for Total Knee Arthroplasty FDA UDI
Model / Reference
Knee+ FDA UDI
Description
Kit of reusable instruments for Total Knee Arthroplasty FDA UDI

Identifiers

Catalog Number
KNK005 FDA UDI
Primary DI / UDI-DI
03760297030339 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

KneeTools V5 Kit by Pixee Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pixee Medical

Sources (1)

  • FDA UDI de15cac9-f2f0-4766-828b-5943b75363c2 35 fields · synced Jun 8, 2026