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Consensus Hip System

FDA UDI

Class II (US FDA UDI)

by Shalby Advanced Technologies, Inc.

Identity

Trade Name
Consensus Hip System FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
Femoral Stem, Collared, Cementless, PC, 12 FDA UDI
Model / Reference
1710-0-0012 FDA UDI
Description
Femoral Stem, Collared, Cementless, PC, 12 FDA UDI

Identifiers

Catalog Number
1710-0-0012 FDA UDI
Primary DI / UDI-DI
00840286809870 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

Consensus 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 3c904b62-1433-4332-a800-455e3b01776a 35 fields · synced May 31, 2026