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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

754565P — Class IIa MDR by Ortopedia y Cirugía, S.L.

MD Atlas
Ortopedia y Cirugía, S.L.

EUDAMED last updated this device on May 25, 2026

754565P

84350815CPNEQW

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ortopedia y Cirugía, S.L.
UDI-DI code: 08435081545652
Reference / catalog number: 754565P

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View device family (Basic UDI)

Manufacturer information

Organization name: Ortopedia y Cirugía, S.L.
SRN: ES-MF-000016977
Manufacturer status: Active

Critical warnings

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

CW999
Producto no estéril. Envasar en sala clase ISO 8 Esterilizar antes de su uso en envase adecuado Método recomendado de esterilización: vapor 134º 8'

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 25, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435081545652
Basic UDI-DI: 84350815CPNEQW
Reference / catalog number: 754565P
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: COMPRESA PLEGADA 50X50 (10X10) 17H 16C
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08435081545652

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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.

M0201020102COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE

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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Certificates

Certificate health across this manufacturer's portfolio.

2024 PR 0016Issued
Quality assuranceNotified body: 0318Expiry: Feb 18, 2029