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Symmcora permanent

by Assut Europe SpA 38 variants

Ref G4017ABB

Symmcora permanent (G4017ABB) is a Class III device made by Assut Europe SpA, registered in EUDAMED on 6 Nov 2024 (Basic UDI-DI 8033439FILBLOCPERMHW) with CE/MDR certificate CSQ0013236826 valid until 7 Aug 2028, active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

7 Aug 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

3 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0013236826 Date26 Oct 2026IssuedStatusActive expires 7 Aug 2028

Official records

Certificates

3 certificates · EUDAMED

EUDAMED certificates (3)
  • CSQ0013236626 Active Supplemented Removed from EUDAMED

    Quality management system EU MDR

    Certifier
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    28 Sep 2026
    Expires
    7 Aug 2028
    Reason
    Add device or group
  • CSQ0013236826 Active Supplemented

    Quality management system EU MDR

    Certifier
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    26 Oct 2026
    Expires
    7 Aug 2028
    Reason
    Add device or group
  • CVD0030240124 Active Supplemented

    Technical documentation EU MDR

    Certifier
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    31 Jul 2024
    Expires
    7 Aug 2028
    Reason
    Add device or group

Timeline

5 dated events

  1. Certificate issued EUDAMED CVD0030240124
  2. Registered EUDAMED 8033439FILBLOCPERMHW
  3. Certificate issued EUDAMED CSQ0013236826
  4. Certificate expires EUDAMED CSQ0013236826
  5. Certificate expires EUDAMED CVD0030240124

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Filbloc Permanent
Model / reference
G4017ABB
Primary DI / UDI-DI
18033439376599
Basic UDI-DI
8033439FILBLOCPERMHW
Direct marketing DI
18033439376599
EMDN code
H010201010401 Polypropylene monofilament with needle for open surgery
Device class
Class III
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000018178

Similar devices in this category

Other devices filed under POLYPROPYLENE MONOFILAMENT WITH NEEDLE FOR OPEN SURGERY.

Other devices from Assut Europe SpA

See all devices from Assut Europe SpA →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)