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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

0SLD700C1A — Class IIb MDR by SILDEHA Pharma Srl

MD Atlas
SILDEHA Pharma Srl

EUDAMED last updated this device on Apr 2, 2026

0SLD700C1A

805720449TLYSCREDERXR

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SILDEHA Pharma Srl
UDI-DI code: 08057204490009
Reference / catalog number: 0SLD700C1A

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View device family (Basic UDI)

Manufacturer information

Organization name: SILDEHA Pharma Srl
SRN: IT-MF-000026622
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW999
Do not use beyond the expiry date. The expiry date on the label refers to the product closed and correctly stored. Do not use if the package is open or damaged.

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	Sep 6, 2023	Still on market
Spain	Nov 7, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057204490009
Basic UDI-DI: 805720449TLYSCREDERXR
Reference / catalog number: 0SLD700C1A
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 30 MU03

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08057204490009

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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.

M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - 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

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Related devices

0SLD700C2G805720449TLYSCREPRO2ROn the market 0SLD700C3B805720449TLYSCRERIN26On 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.