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Delta Xtend

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
Delta Xtend FDA UDI
Generic Name
Total reverse shoulder prosthesis FDA UDI
Device Name
Delta Xtend REVERSE SHOULDER SYSTEM CENTRAL SCREW METAGLENE COLLET Implant: Titanium / Handle: Polycarbonate FDA UDI
Model / Reference
1309-60-111 FDA UDI
Description
Delta Xtend REVERSE SHOULDER SYSTEM CENTRAL SCREW METAGLENE COLLET Implant: Titanium / Handle: Polycarbonate FDA UDI

Identifiers

Catalog Number
130960111 FDA UDI
Primary DI / UDI-DI
10603295525189 FDA UDI
FDA Product Code
KWS FDA UDI
PHX FDA UDI
GMDN Term
Total reverse shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Total reverse shoulder prosthesis

Delta Xtend by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total reverse shoulder prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 7e56ece5-0e08-4a7d-8ce9-1f59eb9b5776 35 fields · synced May 29, 2026