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Arthrex®

FDA UDI

Class II (US FDA UDI)

by Arthrex, Inc.

Identity

Trade Name
Arthrex® FDA UDI
Generic Name
Uncoated shoulder humeral stem prosthesis FDA UDI
Device Name
UNIVERS CA HUMERAL HEAD, 46/18 FDA UDI
Model / Reference
AR-9146-18CA FDA UDI
Description
UNIVERS CA HUMERAL HEAD, 46/18 FDA UDI

Identifiers

Catalog Number
AR-9146-18CA FDA UDI
Primary DI / UDI-DI
00888867136052 FDA UDI
FDA Product Code
HSD FDA UDI
PHX FDA UDI
KWS FDA UDI
GMDN Term
Uncoated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 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

No

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
MRI Safety
MR Conditional FDA UDI

Category: Uncoated shoulder humeral stem prosthesis

Arthrex® by Arthrex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated shoulder humeral stem prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arthrex, Inc.

Sources (1)

  • FDA UDI 2091b939-4c2a-42f9-9727-fa2e4e3bf12c 35 fields · synced Jun 6, 2026