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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

Compressive bandage after knee… — Class I MDR

MD Atlas
UAB Ortopedijos klinika

EUDAMED last updated this device on May 26, 2026

Compressive bandage after knee surgery ORTOPEDIJOS KLINIKA "KT3-8"

4772165OK0135

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: UAB Ortopedijos klinika
UDI-DI code: 04772165000404
Reference / catalog number: Compressive bandage after knee surgery ORTOPEDIJOS KLINIKA "KT3-8"

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View device family (Basic UDI)

Manufacturer information

Organization name: UAB Ortopedijos klinika
SRN: LT-MF-000004389
Manufacturer status: Active

Related devices

UFS4772165OK0339On the market UFS4772165OK0339On the market UFS4772165OK0339On the market UFS4772165OK0339On the market UFS4772165OK0339On the market

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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Lithuania; available across 1 country total.

Country	On market since	Until
LithuaniaPrimary placement	May 1, 2004	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04772165000404
Basic UDI-DI: 4772165OK0135
Reference / catalog number: Compressive bandage after knee surgery ORTOPEDIJOS KLINIKA "KT3-8"
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: Kelio įtvaras
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)04772165000404

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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.

Y061209KNEE 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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