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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

ABD shoulder immobilizer, size M — Class I MDR

MD Atlas
Timago International Group Ossowski Spółka komandytowa

EUDAMED last updated this device on May 28, 2026

ABD shoulder immobilizer, size M

590298372O05148H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Timago International Group Ossowski Spółka komandytowa
UDI-DI code: 05902983722526
Reference / catalog number: TGO-C OB 306_M

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Manufacturer information

Organization name: Timago International Group Ossowski Spółka komandytowa
SRN: PL-MF-000004105
Manufacturer status: Active

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Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: ABD shoulder immobilizer, size M
UDI-DI code: 05902983722526
Basic UDI-DI: 590298372O05148H
Reference / catalog number: TGO-C OB 306_M
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: 1
Additional product description: ABD shoulder immobilizer is used after physical injuries of glenohumeral joint. The immobilizer is used to relieve and stabilize glenohumeral joint in frontal plane position and to align humerus bone in intermediate position.
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)05902983722526

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UDI-PI DataMatrix

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

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EMDN nomenclature code(s)

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

Y060621SHOULDER ORTHOSES

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

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.