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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
Bipolar femoral head outer component, hemiarthroplasty FDA UDI
Device Name
Bipolar Assembly, 28mm×51mm, -5mm FDA UDI
Model / Reference
1020-0-1851 FDA UDI
Description
Bipolar Assembly, 28mm×51mm, -5mm FDA UDI

Identifiers

Catalog Number
1020-0-1851 FDA UDI
Primary DI / UDI-DI
00840286804097 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Bipolar femoral head outer component, hemiarthroplasty FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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: Bipolar femoral head outer component, hemiarthroplasty

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 Bipolar femoral head outer component, hemiarthroplasty.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d38c7928-1d7d-4b59-9994-b0bc9d969276 35 fields · synced May 30, 2026