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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

Tubicodo tubular stretch bandage T2 — Class I MDR

MD Atlas
COMERCIAL GOMILA-CATALÀ, SL.

EUDAMED last updated this device on Jan 19, 2023

Tubicodo tubular stretch bandage T2

8437023007VEXTENSSW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: COMERCIAL GOMILA-CATALÀ, SL.
UDI-DI code: 08437023007136
Reference / catalog number: 12.202

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Manufacturer information

Organization name: COMERCIAL GOMILA-CATALÀ, SL.
SRN: ES-MF-000004307
Manufacturer status: Active

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Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: Tubicodo tubular stretch bandage T2
UDI-DI code: 08437023007136
Basic UDI-DI: 8437023007VEXTENSSW
Reference / catalog number: 12.202
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: Continuous tubular stretcht bandage, non-compressive restraint.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03030103TUBULAR NET BANDAGES

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.