← Back to catalogue

Delta Xtend Cta

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2307-82-001Model Orthopaedic Reamer Guide

by DePuy Ireland UC

Identity

Trade Name
DELTA XTEND CTA EUDAMED
DELTA XTEND FDA UDI
Generic Name
Orthopaedic reamer guide FDA UDI
Device Name
Orthopaedic Reamer Guide EUDAMED
DELTA Xtend DELTA CTA HEAD REAMING GUIDE FDA UDI
Model / Reference
Orthopaedic Reamer Guide EUDAMED
2307-82-001 EUDAMEDFDA UDI
Description
DELTA Xtend DELTA CTA HEAD REAMING GUIDE FDA UDI

Identifiers

Catalog Number
230782001 FDA UDI
Primary DI / UDI-DI
10603295116349 EUDAMEDFDA UDI
Basic UDI-DI
0603295a004278W EUDAMED
Direct Marketing DI
10603295116349 EUDAMED
FDA Product Code
HWT FDA UDI
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic reamer guide FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4800 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Bone cutting forceps, reusable

Delta Xtend Cta by DePuy Ireland UC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
DePuy Ireland UC
EUDAMED SRN
IE-MF-000007377

Sources (2)

  • EUDAMED 655911ef-96dd-4707-a029-9e27136d0960 61 fields · synced Jun 19, 2026
  • FDA UDI f3dd1b4f-61b8-4e47-8855-7cc0a6b87797 35 fields · synced May 29, 2026