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Delta Xtend

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
DELTA XTEND FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
DELTA Xtend GLENOID CASE TOP TRAY R2 FDA UDI
Model / Reference
240799936 FDA UDI
Description
DELTA Xtend GLENOID CASE TOP TRAY R2 FDA UDI

Identifiers

Catalog Number
240799936 FDA UDI
Primary DI / UDI-DI
10603295285991 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI b58d9190-ae44-460e-9f9d-5e0bd0f9ec97 35 fields · synced Jun 1, 2026