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LEPORELLO 3.5mm Olecranon Plate 7 Hole, Left
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref B-151200Model LEPORELLO 3.5mm Olecranon Plate
Identity
- Trade Name
- LEPORELLO 3.5mm Olecranon Plate 7 Hole, Left EUDAMEDFDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
- Device Name
- LEPORELLO EUDAMED
- Model / Reference
- LEPORELLO 3.5mm Olecranon Plate EUDAMEDB-151200 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 07640187462616 EUDAMEDFDA UDI
- Basic UDI-DI
- 764018746LEPORELLOWT EUDAMED
- Direct Marketing DI
- 07640187462616 EUDAMED
- 510(k) Number
- K243308 FDA UDI
- FDA Product Code
- HRS FDA UDI
- EMDN Code
- P09120699 BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS - OTHER EUDAMEDP09120599 BONE FIXATION PLATES - OTHER EUDAMED
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Sutures
Yes
EUDAMED
CMR Substance
No
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
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
MR Conditional FDA UDI
LEPORELLO 3.5mm Olecranon Plate 7 Hole, Left by Bonebridge AG — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 764018746LEPORELLOWT | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Bonebridge AG
- EUDAMED SRN
- CH-MF-000013933
- Authorised Representative
- Axxos GmbH DE-AR-000005590
Sources (3)
- EUDAMED 59cecd4c-65f2-48cd-95f8-077ece05569f 61 fields · synced Jun 19, 2026
- FDA UDI 7ba11868-ac08-4b3c-8b6b-e2a9d215851e 33 fields · synced May 30, 2026
- EUDAMED 2c23adc5-462b-48f0-aac1-b48be1e84b66 61 fields · synced Jun 19, 2026