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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

Sanipore Salvelox Banda Fix 75X8cm — Class I MDR

MD Atlas
Orkla Cederroth, SAU

EUDAMED last updated this device on Jun 6, 2024

Sanipore Salvelox Banda Fix 75X8cm

8414797TF08NWFIBG3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orkla Cederroth, SAU
UDI-DI code: 08470003732826
Reference / catalog number: 309885

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Manufacturer information

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

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW009
This product is for single use only.

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: Sanipore Salvelox Banda Fix 75X8cm
UDI-DI code: 08470003732826
Basic UDI-DI: 8414797TF08NWFIBG3
Reference / catalog number: 309885
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: EA reference: 451181311 SANIPORE BAND FIX 75X8 R 1X1 Cs reference: 309885 Sanipore Salvelox Banda FIX 75X8cm 10X1 Sensitive skins. Elastic non woven dressing band for cutting. Hypo-allergenic and elastic. Dimensions: 0'75m x 8cm.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M04010101NON-WOVEN ADHESIVE DRESSINGS, WITH ABSORBENT PAD

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

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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.