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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

CERCLAGE WIRE — Class IIb MDR by SURGIVAL CO., S.A.U.

MD Atlas
SURGIVAL CO., S.A.U.

EUDAMED last updated this device on May 5, 2026

CERCLAGE WIRE

84352258IMP30200002S

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SURGIVAL CO., S.A.U.
UDI-DI code: 08435225819366
Reference / catalog number: C6113001

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Manufacturer information

Organization name: SURGIVAL CO., S.A.U.
SRN: ES-MF-000028629
Manufacturer status: Active

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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.

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 3 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Italy		Still on market
Portugal		Still on market

Device identification

Trade name: CERCLAGE WIRE
UDI-DI code: 08435225819366
Basic UDI-DI: 84352258IMP30200002S
Reference / catalog number: C6113001
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: https://eifu.surgival.com/
Clinical sizes: 1 MU50
10 MU36

EMDN nomenclature code(s)

P09120302CERCLAGE DEVICES, WIRES AND BINDERS

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