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TaperSet™ Hip System

FDA UDI

Class II (US FDA UDI)

by Shalby Advanced Technologies, Inc.

Identity

Trade Name
TaperSet™ Hip System FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
Femoral Stem, Standard, Cementless, PC, Plasma, 6mm FDA UDI
Model / Reference
1210-0-0060 FDA UDI
Description
Femoral Stem, Standard, Cementless, PC, Plasma, 6mm FDA UDI

Identifiers

Catalog Number
1210-0-0060 FDA UDI
Primary DI / UDI-DI
00840286807357 FDA UDI
FDA Product Code
KWL FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Coated femoral stem prosthesis, modular

TaperSet™ Hip System by Shalby Advanced Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2ea6d165-c5a5-4ebc-988b-0752535fa9f0 35 fields · synced Jun 8, 2026