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UniSyn Hip System

FDA UDI

Class II (US FDA UDI)

by Shalby Advanced Technologies, Inc.

Identity

Trade Name
UniSyn Hip System FDA UDI
Generic Name
Revision coated hip femur prosthesis FDA UDI
Device Name
Body, Standard, Cementless, PC, HA/Plasma, 32mm, 38mm FDA UDI
Model / Reference
3461-53238-A FDA UDI
Description
Body, Standard, Cementless, PC, HA/Plasma, 32mm, 38mm FDA UDI

Identifiers

Catalog Number
3461-53238-A FDA UDI
Primary DI / UDI-DI
00840286837705 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Revision coated hip femur prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 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: Revision coated hip femur prosthesis

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

Similar devices

Also classified as Revision coated hip femur prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e4a1a6fd-6ed6-40b8-b7c3-a36e7af79491 35 fields · synced May 31, 2026