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Delta Xtend
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2307-73-003Model Osteotomy Guide, Reusable
Identity
- Trade Name
- DELTA XTEND EUDAMEDFDA UDI
- Generic Name
- Osteotomy guide, reusable FDA UDI
- Device Name
- Osteotomy Guide, Reusable EUDAMEDDELTA Xtend SUPERIOR LATERAL CUTTING GUIDE FDA UDI
- Model / Reference
- Osteotomy Guide, Reusable EUDAMED2307-73-003 EUDAMEDFDA UDI
- Description
- DELTA Xtend SUPERIOR LATERAL CUTTING GUIDE FDA UDI
Identifiers
- Catalog Number
- 230773003 FDA UDI
- Primary DI / UDI-DI
- 10603295116103 EUDAMEDFDA UDI
- Basic UDI-DI
- 0603295a004288Y EUDAMED
- Direct Marketing DI
- 10603295116103 EUDAMED
- FDA Product Code
- HWT FDA UDI
- EMDN Code
- L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Osteotomy guide, reusable 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
Moist Heat or Steam Sterilization FDA UDI
Category: Bone cutting forceps, reusable
Delta Xtend by DePuy Ireland UC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0603295a004288Y | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- DePuy Ireland UC
- EUDAMED SRN
- IE-MF-000007377
Sources (2)
- EUDAMED 3f97c6da-4aa7-43ad-9a8c-ceffb139d99c 61 fields · synced May 30, 2026
- FDA UDI 3af815e9-af96-4b22-abdd-2ac6b8350b81 35 fields · synced May 30, 2026