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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

1731GD — Class I MDR by ORTOTEX MEDICAL S.L.

MD Atlas
ORTOTEX MEDICAL S.L.

EUDAMED last updated this device on Mar 18, 2025

1731GD

843702443305CQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ORTOTEX MEDICAL S.L.
UDI-DI code: 08437024433446
Reference / catalog number: 1731GD

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Manufacturer information

Organization name: ORTOTEX MEDICAL S.L.
SRN: ES-MF-000011654
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437024433446
Basic UDI-DI: 843702443305CQ
Reference / catalog number: 1731GD
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: The Lambskin anti-bedsore boot ORTOTEX MEDICAL has the following main properties: Chrome-free, tanned with natural products that do not irritate the skin. Fire-resistant function. Reduces friction and slippage. Hygroscopic function, absorbs moisture generated by perspiration (approximately 30%). Reduces pressure, promoting proper ventilation of the affected area. Preventive and supportive function. Maintains resistance, density, and softness for a long time. It is indicated for preventing the appearance of pressure ulcers due to restricted blood flow caused by the localized compression of soft tissue arterial networks.
Additional information URL: https://ortotexmedical.com/producto/bota-lambskin/
Clinical sizes: 8.5 MU10
18.5 MU10
25 MU10

EMDN nomenclature code(s)

V0811HEEL, ELBOW AND KNEE ANTI-DECUBITUS PROTECTION AIDS

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

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.

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