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LEPORELLO 3.5mm Olecranon Plate, 5 Hole, Right

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref B-152000Model LEPORELLO 3.5mm Olecranon Plate

by Bonebridge AG

Identity

Trade Name
LEPORELLO 3.5mm Olecranon Plate, 5 Hole, Right EUDAMEDFDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
LEPORELLO EUDAMED
Model / Reference
LEPORELLO 3.5mm Olecranon Plate EUDAMED
B-152000 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07640187461947 EUDAMEDFDA UDI
Basic UDI-DI
764018746LEPORELLOWT EUDAMED
Direct Marketing DI
07640187461947 EUDAMED
510(k) Number
K213864 FDA UDI
FDA Product Code
HRS FDA UDI
EMDN Code
P09120599 BONE FIXATION PLATES - OTHER EUDAMED
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class 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
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

LEPORELLO 3.5mm Olecranon Plate, 5 Hole, Right by Bonebridge AG — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bonebridge AG
EUDAMED SRN
CH-MF-000013933
Authorised Representative
Axxos GmbH DE-AR-000005590

Sources (2)

  • EUDAMED 19eae551-bc04-4cc6-bf3e-b14da24f9af4 61 fields · synced Jul 10, 2026
  • FDA UDI b058e698-4a76-4c23-b81b-3476dcdbafe4 33 fields · synced May 30, 2026