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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

ID 313 — Class I MDR by Handicap trade s.r.o.

MD Atlas
Handicap trade s.r.o.

EUDAMED last updated this device on May 29, 2026

ID 313

859420903001H2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Handicap trade s.r.o.
UDI-DI code: 08594209030002
Reference / catalog number: ID 313

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View device family (Basic UDI)

Manufacturer information

Organization name: Handicap trade s.r.o.
SRN: CZ-MF-000016787
Manufacturer status: Active

Related devices

ID 312859420903001H2On the market ID 504859420903001H2On the market TDH859420903011H5On the market TDH859420903011H5On the market TDH859420903011H5On 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 Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594209030002
Basic UDI-DI: 859420903001H2
Reference / catalog number: ID 313
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: Berle francouzská dětská FDD 91 Handicap je určena k odlehčení dolní končetiny a/nebo zajištění stability při nemožnosti užití standartní bipedální lokomoce u dětských pacientů či pacientů menšího vzrůstu.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Dospělá rukojeť šedá

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08594209030002

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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.

Y12030601ELBOW CRUTCHES

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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