EUDAMED last updated this device on May 27, 2026

754545Z

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: 08435081545454
Reference / catalog number: 754545Z

754545Z is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Ortopedia y Cirugía, S.L.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 27, 2026

754545Z

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: 08435081545454
Reference / catalog number: 754545Z

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 08435081545454
Basic UDI-DI: 84350815CPNEQW
Reference / catalog number: 754545Z
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 20X30 17H 8C RX PLEG.SEGURIDAD
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)08435081545454

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M0201020202COTTON GAUZES, FOLDED, WITH X-RAY DETECTABLE THREAD, NON-STERILE

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'

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

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 27, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435081545454
Basic UDI-DI: 84350815CPNEQW
Reference / catalog number: 754545Z
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 20X30 17H 8C RX PLEG.SEGURIDAD
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08435081545454

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M0201020202COTTON GAUZES, FOLDED, WITH X-RAY DETECTABLE THREAD, NON-STERILE

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'

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

Certificates

Certificate health across this manufacturer's portfolio.

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

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

All products by Ortopedia y Cirugía, S.L.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 27, 2026	Still on market

754545Z

754545Z

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Related devices