EUDAMED last updated this device on Jul 1, 2026

BEPOD PERCUTANEOUS HINDFOOT OSTEOTOMY BONE LEVER

3661489PIEDCIRM97

On the marketClass I

Applicable legislation: —
Organization name: FOURNITURES HOSPITALIERES INDUSTRIE
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 03661489722813
Reference / catalog number: 272281

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

BEPOD PERCUTANEOUS HINDFOOT OSTEOTOMY BONE LEVER is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by FOURNITURES HOSPITALIERES INDUSTRIE. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: BEPOD PERCUTANEOUS HINDFOOT OSTEOTOMY BONE LEVER
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 03661489722813
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: 3661489PIEDCIRM97
Reference / catalog number: 272281
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class I
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)03661489722813

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in France; available across 10 countries total.

Country	On market since	Until
FrancePrimary placement	—	Still on market
Austria	—	Still on market
Belgium	—	Still on market
Bulgaria	—	Still on market
Germany	—	Still on market
Spain	—	Still on market
Italy	—	Still on market
Poland	—	Still on market
Portugal	—	Still on market
Slovenia	—	Still on market

Related searches

Class I medical devices in EUDAMED

Device identification

Trade name: BEPOD PERCUTANEOUS HINDFOOT OSTEOTOMY BONE LEVER
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 03661489722813
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: 3661489PIEDCIRM97
Reference / catalog number: 272281
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Certificates

Certificate health across this manufacturer's portfolio.

40595Issued
Quality management system
Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
: GMED SAS (0459)Expiry: Apr 11, 2027
40599Issued
Quality management system
Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
: GMED SAS (0459)Expiry: Apr 11, 2027
40594Issued
Quality management system
Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
: GMED SAS (0459)Expiry: Apr 11, 2027
40362Amended
Quality management system
Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
: GMED SAS (0459)Expiry: Apr 11, 2027
40417Amended
Quality management system
Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
: GMED SAS (0459)Expiry: Apr 11, 2027
38944Supplemented
Quality management system: GMED SAS (0459)Expiry: Apr 11, 2027

Market distribution

Primary placement in France; available across 10 countries total.

Country	On market since	Until
FrancePrimary placement	—	Still on market
Austria	—	Still on market
Belgium	—	Still on market
Bulgaria	—	Still on market
Germany	—	Still on market
Spain	—	Still on market
Italy	—	Still on market
Poland	—	Still on market
Portugal	—	Still on market
Slovenia	—	Still on market

BEPOD PERCUTANEOUS HINDFOOT OSTEOTOMY BONE LEVER

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Certificates covering this device

Related devices