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Aptos

by Aptos LLC

Ref AW3.0034Model Body Wire Method 3/0

Aptos (AW3.0034) is a Class IIa device made by Aptos, LLC, registered in EUDAMED on 29 Jan 2026 (Basic UDI-DI B-4860120240108), active as of 23 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-4860120240108 Basic UDI-DI 4860120240108UDI-DIDate29 Jan 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Aptos Instruments
Model / reference
Body Wire Method 3/0, AW3.0034
Primary DI / UDI-DI
4860120240108
Basic UDI-DI
B-4860120240108
EMDN code
H010202020101 Stainless steel multifilament with needle
Device class
Class IIa
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
GE-MF-000020012
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under NON-ABSORBABLE NON-SYNTHETIC MULTIFILAMENT SUTURES.

Other devices from Aptos, LLC

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Properties

  • Supplied sterile
  • Sterilise before use
Other properties (10, all answered No)