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Monofil Fast

by Assut Europe SpA 239 variants

Part of a family of 249 devices: see the family page

Ref FR574QAP

Monofil Fast (FR574QAP) is a Class III device made by Assut Europe SpA, registered in EUDAMED on 27 May 2025 (Basic UDI-DI 8033439MONOFILFAST2K) with CE/MDR certificate CSQ0013236826 valid until 7 Aug 2028, active as of 23 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

4 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

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

Official records

Certificates

4 certificates · EUDAMED

EUDAMED certificates (4)
  • CSQ0013236626 Active Supplemented Removed from EUDAMED

    Quality management system EU MDR

    Issued
    28 Sep 2026
    Expires
    7 Aug 2028
    Reason
    Add device or group
  • CSQ0013236826 Active Supplemented

    Quality management system EU MDR

    Issued
    26 Oct 2026
    Expires
    7 Aug 2028
    Reason
    Add device or group
  • CVD0044250226 Active Supplemented Removed from EUDAMED

    Technical documentation EU MDR

    Issued
    6 Feb 2026
    Expires
    7 Aug 2028
    Reason
    Change approved
  • CVD0044250426 Active Supplemented

    Technical documentation EU MDR

    Issued
    26 Oct 2026
    Expires
    7 Aug 2028
    Reason
    Add device or group

Timeline

5 dated events

  1. Registered EUDAMED 8033439MONOFILFAST2K
  2. Certificate issued EUDAMED CSQ0013236826
  3. Certificate issued EUDAMED CVD0044250426
  4. Certificate expires EUDAMED CSQ0013236826
  5. Certificate expires EUDAMED CVD0044250426

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
FR574QAP
Primary DI / UDI-DI
38033439429657
Basic UDI-DI
8033439MONOFILFAST2K
Direct marketing DI
38033439429657
EMDN code
H010101010301 Poliglecaprone and derivatives monofilament with needle
Device class
Class III
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000018178

Similar devices in this category

Other devices filed under POLIGLECAPRONE AND DERIVATIVES MONOFILAMENT WITH NEEDLE.

Other devices from Assut Europe SpA

See all devices from Assut Europe SpA →

Properties

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