EUDAMED last updated this device on May 29, 2026

0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg

76300378022PA

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medartis AG
UDI-DI code: 07630037864349
Reference / catalog number: A-5043.90/1

0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Medartis AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 29, 2026

0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg

76300378022PA

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medartis AG
UDI-DI code: 07630037864349
Reference / catalog number: A-5043.90/1

View device family (Basic UDI)

Device identification

Trade name: 0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg
UDI-DI code: 07630037864349
Basic UDI-DI: 76300378022PA
Reference / catalog number: A-5043.90/1
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://ifu.medartis.com/
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)07630037864349

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.

P09120699BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS - OTHER

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW007
Do not use if package is damaged
CW009
Do not re-use
CW010
Consult instructions for use
CW026
MR CONDITIONAL

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in Germany; available across 29 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market
Belgium		Still on market
Bulgaria		Still on market
Cyprus		Still on market
Czechia		Still on market
Denmark		Still on market
Estonia		Still on market
EL		Still on market
Spain		Still on market
Finland		Still on market
France		Still on market
Croatia		Still on market
Hungary		Still on market
Ireland		Still on market
Italy		Still on market
Liechtenstein		Still on market
Lithuania		Still on market
Luxembourg		Still on market
Latvia		Still on market
Malta		Still on market
Netherlands		Still on market
Norway		Still on market
Poland		Still on market
Portugal		Still on market
Romania		Still on market
Sweden		Still on market
Slovenia		Still on market
Slovakia		Still on market

Device identification

Trade name: 0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg
UDI-DI code: 07630037864349
Basic UDI-DI: 76300378022PA
Reference / catalog number: A-5043.90/1
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://ifu.medartis.com/
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Medartis AG
SRN: CH-MF-000022291
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07630037864349

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.

P09120699BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS - OTHER

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW007
Do not use if package is damaged
CW009
Do not re-use
CW010
Consult instructions for use
CW026
MR CONDITIONAL

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Certificates

Certificate health across this manufacturer's portfolio.

HZ 1809678-1Supplemented
Quality management systemNotified body: 0197Expiry: Dec 29, 2026

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

All products by Medartis AG

Market distribution

Primary placement in Germany; available across 29 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market
Belgium		Still on market
Bulgaria		Still on market
Cyprus		Still on market
Czechia		Still on market
Denmark		Still on market
Estonia		Still on market
EL		Still on market
Spain		Still on market
Finland		Still on market
France		Still on market
Croatia		Still on market
Hungary		Still on market
Ireland		Still on market
Italy		Still on market
Liechtenstein		Still on market
Lithuania		Still on market
Luxembourg		Still on market
Latvia		Still on market
Malta		Still on market
Netherlands		Still on market
Norway		Still on market
Poland		Still on market
Portugal		Still on market
Romania		Still on market
Sweden		Still on market
Slovenia		Still on market
Slovakia		Still on market

0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg

0.6 K-Wire, Trocar, 2-end. 100mm,1/Pkg

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

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

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Related devices