Delta Xtend

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name: DELTA XTEND FDA UDI
Generic Name: Bone-resection orthopaedic reamer, reusable FDA UDI
Device Name: DELTA XTEND Central Screw Metaglene augmented metaglene reamer half wedge stop foot FDA UDI
Model / Reference: 2317-70-524 FDA UDI
Description: DELTA XTEND Central Screw Metaglene augmented metaglene reamer half wedge stop foot FDA UDI

Identifiers

Catalog Number: 231770524 FDA UDI
Primary DI / UDI-DI: 10603295532781 FDA UDI
FDA Product Code: KIJ FDA UDI
GMDN Term: Bone-resection orthopaedic reamer, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone-resection orthopaedic reamer, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Depuy (ireland)

Sources (1)

FDA UDI c2444b2d-4047-4507-8551-8c8bc52d7517 35 fields · synced May 31, 2026