EUDAMED last updated this device on Jun 5, 2026

1431

7331791-COM-0-000-0004-5B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Atos Medical AB
UDI-DI code: 07331791006784
Reference / catalog number: 1431

1431 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Atos Medical AB. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on Jun 5, 2026

1431

7331791-COM-0-000-0004-5B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Atos Medical AB
UDI-DI code: 07331791006784
Reference / catalog number: 1431

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 07331791006784
Basic UDI-DI: 7331791-COM-0-000-0004-5B
Reference / catalog number: 1431
Issuing entity: GS1

Classification

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

Device details

Quantity: 10
Additional product description: Tracheostomy tube dressing
Additional information URL: https://www.atosmedical.com/
Clinical sizes: 70 MU50
65 MU50
Thickness — 3.5 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07331791006784

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.

M0499SPECIAL DRESSINGS - 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 Austria; available across 21 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Belgium		Still on market
Germany		Still on market
Denmark		Still on market
Spain		Still on market
Finland		Still on market
France		Still on market
Croatia		Still on market
Hungary		Still on market
Liechtenstein		Still on market
Lithuania		Still on market
Luxembourg		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
Slovakia		Still on market
XI		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07331791006784
Basic UDI-DI: 7331791-COM-0-000-0004-5B
Reference / catalog number: 1431
Issuing entity: GS1

Classification

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

Device details

Quantity: 10
Additional product description: Tracheostomy tube dressing
Additional information URL: https://www.atosmedical.com/
Clinical sizes: 70 MU50
65 MU50
Thickness — 3.5 MU50

Manufacturer information

Organization name: Atos Medical AB
SRN: SE-MF-000000725
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07331791006784

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.

M0499SPECIAL DRESSINGS - 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.

C520850Issued
Quality management systemNotified body: 2460Expiry: Feb 11, 2030

Certificates covering this device

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

All products by Atos Medical AB

Market distribution

Primary placement in Austria; available across 21 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Belgium		Still on market
Germany		Still on market
Denmark		Still on market
Spain		Still on market
Finland		Still on market
France		Still on market
Croatia		Still on market
Hungary		Still on market
Liechtenstein		Still on market
Lithuania		Still on market
Luxembourg		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
Slovakia		Still on market
XI		Still on market

1431

1431

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