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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

Salvequick Silicone Tube EXP 12X1 — Class I MDR

MD Atlas
Orkla Cederroth, SAU

EUDAMED last updated this device on Jul 13, 2023

Salvequick Silicone Tube EXP 12X1

8414797TF15TUPRPLA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orkla Cederroth, SAU
UDI-DI code: 07310610020163
Reference / catalog number: 51030143

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Manufacturer information

Organization name: Orkla Cederroth, SAU
SRN: ES-MF-000003606
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

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

CW011
Do not wear over open wounds and keep out of the reach of children.
CW999
Wear the product no more than 16 hours a day.
CW030
Individuals with diabetes and with poor blood circulation should consult their doctor.

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: Salvequick Silicone Tube EXP 12X1
UDI-DI code: 07310610020163
Basic UDI-DI: 8414797TF15TUPRPLA
Reference / catalog number: 51030143
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 tubes with inner gel coating offer protection and relief against corns and toe chafing, in addition to preventing the appearance of new corns.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 15 MU10
20 MU50

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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Expiration date
Manufacturing date
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Software identification