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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

M260ES — Class IIa MDR by Serrix B.V

MD Atlas
Serrix B.V

EUDAMED last updated this device on Mar 5, 2026

M260ES

871830970M2X0EGCW

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Serrix B.V
UDI-DI code: 08718309703011
Reference / catalog number: M260ES

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View device family (Basic UDI)

Manufacturer information

Organization name: Serrix B.V
SRN: NL-MF-000005882
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

BE23/00000172Supplemented
Quality management systemNotified body: 1639Expiry: Jun 19, 2028

Critical warnings

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

CW010
Consult instruction for use (symbol)
CW262
Single patient, multiple use (symbol)
CW275
When pregnant or breastfeeding, only use if instructed by and under supervision of a health care professional

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08718309703011
Basic UDI-DI: 871830970M2X0EGCW
Reference / catalog number: M260ES
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: —
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)08718309703011

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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.

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

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