EUDAMED last updated this device on Jun 26, 2026

4.5250.600S

59084474SP24F

On the marketClass IIb

Applicable legislation: —
Organization name: ChM spółka z ograniczoną odpowiedzialnością
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 →: 05908447603363
Reference / catalog number: 4.5250.600S

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.

4.5250.600S is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by ChM spółka z ograniczoną odpowiedzialnością. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: not provided
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 →: 05908447603363
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 →: 59084474SP24F
Reference / catalog number: 4.5250.600S
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 IIb
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Catalogue no: 4.5250.600S Cerclage cable with clamp 2.0x600
Additional information URL: https://ifu.chm.eu/
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)05908447603363

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.

P09120399BONE FIXATION WIRES - OTHER

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

Consult instructions for use

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Poland; available across 17 countries total.

Country	On market since	Until
PolandPrimary placement	—	Still on market
Bulgaria	—	Still on market
Cyprus	—	Still on market
Czechia	—	Still on market
Germany	—	Still on market
Estonia	—	Still on market
EL	—	Still on market
Spain	—	Still on market
France	—	Still on market
Croatia	—	Still on market
Italy	—	Still on market
Lithuania	—	Still on market
Latvia	—	Still on market
Portugal	—	Still on market
Romania	—	Still on market
Slovenia	—	Still on market
Slovakia	—	Still on market

Related searches

Class IIb medical devices in EUDAMED

Device identification

Trade name: not provided
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 →: 05908447603363
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 →: 59084474SP24F
Reference / catalog number: 4.5250.600S
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.

HZ 1023642-1Supplemented
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.
: TÜV Rheinland LGA Products GmbH (0197)Expiry: Apr 29, 2030
IZ 1023642-2Issued
Technical documentation
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.
: TÜV Rheinland LGA Products GmbH (0197)Expiry: Jan 18, 2031
IZ 1023642-1Issued
Technical documentation
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.
: TÜV Rheinland LGA Products GmbH (0197)Expiry: Dec 30, 2030

Market distribution

Primary placement in Poland; available across 17 countries total.

Country	On market since	Until
PolandPrimary placement	—	Still on market
Bulgaria	—	Still on market
Cyprus	—	Still on market
Czechia	—	Still on market
Germany	—	Still on market
Estonia	—	Still on market
EL	—	Still on market
Spain	—	Still on market
France	—	Still on market
Croatia	—	Still on market
Italy	—	Still on market
Lithuania	—	Still on market
Latvia	—	Still on market
Portugal	—	Still on market
Romania	—	Still on market
Slovenia	—	Still on market
Slovakia	—	Still on market

4.5250.600S

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