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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

Dr. Frei Pro — Class I MDR by Medtex Swiss Ltd

MD Atlas
Medtex Swiss Ltd

EUDAMED last updated this device on May 19, 2022

Dr. Frei Pro

7640162324588YX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medtex Swiss Ltd
UDI-DI code: 07640162324588
Reference / catalog number: S8321

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Manufacturer information

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

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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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Bulgaria; available across 1 country total.

Placed on the market in Bulgaria; per-country availability dates not published.

Device identification

Trade name: Dr. Frei Pro
UDI-DI code: 07640162324588
Basic UDI-DI: 7640162324588YX
Reference / catalog number: S8321
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 24–30 MU10

EMDN nomenclature code(s)

M03040299ELASTIC SUPPORT BANDAGES - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification