EUDAMED last updated this device on Dec 10, 2025

VEGA SYSTEM PS

40392390000027583F

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aesculap AG
UDI-DI code: 04046963737498
Reference / catalog number: NS356R

VEGA SYSTEM PS is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Aesculap AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

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Country
Date of registration
Address

EUDAMED last updated this device on Dec 10, 2025

VEGA SYSTEM PS

40392390000027583F

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aesculap AG
UDI-DI code: 04046963737498
Reference / catalog number: NS356R

View device family (Basic UDI)

Device identification

Trade name: VEGA SYSTEM PS
UDI-DI code: 04046963737498
Basic UDI-DI: 40392390000027583F
Reference / catalog number: NS356R
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: VEGA PS TIBIA TRIAL/PREPAR.PLATEAU T3+
Additional information URL: https://eifu.bbraun.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)04046963737498

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

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 27 countries total.

Country	On market since	Until
GermanyPrimary placement	Mar 16, 2010	Still on market
Austria	Mar 16, 2010	Still on market
Belgium	Mar 16, 2010	Still on market
Bulgaria	Mar 16, 2010	Still on market
Cyprus	Mar 16, 2010	Still on market
Czechia	Mar 16, 2010	Still on market
Denmark	Mar 16, 2010	Still on market
Estonia	Mar 16, 2010	Still on market
EL	Mar 16, 2010	Still on market
Spain	Mar 16, 2010	Still on market
Finland	Mar 16, 2010	Still on market
France	Mar 16, 2010	Still on market
Croatia	Mar 16, 2010	Still on market
Hungary	Mar 16, 2010	Still on market
Ireland	Mar 16, 2010	Still on market
Italy	Mar 16, 2010	Still on market
Lithuania	Mar 16, 2010	Still on market
Luxembourg	Mar 16, 2010	Still on market
Latvia	Mar 16, 2010	Still on market
Malta	Mar 16, 2010	Still on market
Netherlands	Mar 16, 2010	Still on market
Poland	Mar 16, 2010	Still on market
Portugal	Mar 16, 2010	Still on market
Romania	Mar 16, 2010	Still on market
Sweden	Mar 16, 2010	Still on market
Slovenia	Mar 16, 2010	Still on market
Slovakia	Mar 16, 2010	Still on market

Device identification

Trade name: VEGA SYSTEM PS
UDI-DI code: 04046963737498
Basic UDI-DI: 40392390000027583F
Reference / catalog number: NS356R
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: VEGA PS TIBIA TRIAL/PREPAR.PLATEAU T3+
Additional information URL: https://eifu.bbraun.com/
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Aesculap AG
SRN: DE-MF-000005504
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04046963737498

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

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.

G12 010066 0441Supplemented
Quality management systemNotified body: 0123Expiry: Jun 30, 2026
20334GB450240524Issued
Technical documentationNotified body: 0482Expiry: May 23, 2029
20333GB450240524Issued
Technical documentationNotified body: 0482Expiry: May 23, 2029

Certificates covering this device

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

All products by Aesculap AG

Market distribution

Primary placement in Germany; available across 27 countries total.

Country	On market since	Until
GermanyPrimary placement	Mar 16, 2010	Still on market
Austria	Mar 16, 2010	Still on market
Belgium	Mar 16, 2010	Still on market
Bulgaria	Mar 16, 2010	Still on market
Cyprus	Mar 16, 2010	Still on market
Czechia	Mar 16, 2010	Still on market
Denmark	Mar 16, 2010	Still on market
Estonia	Mar 16, 2010	Still on market
EL	Mar 16, 2010	Still on market
Spain	Mar 16, 2010	Still on market
Finland	Mar 16, 2010	Still on market
France	Mar 16, 2010	Still on market
Croatia	Mar 16, 2010	Still on market
Hungary	Mar 16, 2010	Still on market
Ireland	Mar 16, 2010	Still on market
Italy	Mar 16, 2010	Still on market
Lithuania	Mar 16, 2010	Still on market
Luxembourg	Mar 16, 2010	Still on market
Latvia	Mar 16, 2010	Still on market
Malta	Mar 16, 2010	Still on market
Netherlands	Mar 16, 2010	Still on market
Poland	Mar 16, 2010	Still on market
Portugal	Mar 16, 2010	Still on market
Romania	Mar 16, 2010	Still on market
Sweden	Mar 16, 2010	Still on market
Slovenia	Mar 16, 2010	Still on market
Slovakia	Mar 16, 2010	Still on market

VEGA SYSTEM PS

VEGA SYSTEM PS

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