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Tahoe Unicompartmental Knee System

FDA UDI

Class I (US FDA UDI)

by Shalby Advanced Technologies, Inc.

Identity

Trade Name
Tahoe Unicompartmental Knee System FDA UDI
Generic Name
Orthopaedic instrument extractor FDA UDI
Device Name
Pin Puller, Assy FDA UDI
Model / Reference
2801-0-0532 FDA UDI
Description
Pin Puller, Assy FDA UDI

Identifiers

Catalog Number
2801-0-0532 FDA UDI
Primary DI / UDI-DI
00840286855952 FDA UDI
FDA Product Code
HWB FDA UDI
GMDN Term
Orthopaedic instrument extractor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

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: Orthopaedic instrument extractor

Tahoe Unicompartmental Knee System by Shalby Advanced Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic instrument extractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9947d2e-e505-48b3-b577-56cde54b980d 36 fields · synced May 30, 2026