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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

1602 — Class I MDR by Medtex Swiss Ltd

MD Atlas
Medtex Swiss Ltd

EUDAMED last updated this device on May 11, 2026

1602

380023248B16022CH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medtex Swiss Ltd
UDI-DI code: 03800232485302
Reference / catalog number: 1602

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View device family (Basic UDI)

Manufacturer information

Organization name: Medtex Swiss Ltd
SRN: BG-MF-000023453
Manufacturer status: Active

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Knee high (open foot)380023248B16022CHOn the market Knee high (open foot)380023248B16022CHOn the market Knee high (open foot)380023248B16022CHOn the market Knee high (open toe)380023248B16032CLOn the market Pantyhose (closed toe)380023248B16101CEOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW275
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Bulgaria; available across 1 country total.

Country	On market since	Until
BulgariaPrimary placement	Aug 31, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03800232485302
Basic UDI-DI: 380023248B16022CH
Reference / catalog number: 1602
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: клас на компресия 20-30 mmHg
Additional information URL: https://medtex-swiss.ch/
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)03800232485302

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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.

Y061299LOWER EXTREMITY ORTHOSES - OTHER

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.