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Aptos

by Aptos LLC 6 variants

Ref LLN2GSL016Model Light Lift Needle Method S

Aptos (LLN2GSL016) is a Class III device made by Aptos, LLC, registered in EUDAMED on 23 Jan 2026 (Basic UDI-DI B-4860120240269), 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-4860120240269 Basic UDI-DI 4860120240269UDI-DIDate23 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  • Withdrawn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 Threads - Absorbable Surgical Sutures
Model / reference
Light Lift Needle Method S, LLN2GSL016
Primary DI / UDI-DI
4860120240269
Basic UDI-DI
B-4860120240269
EMDN code
H0101010199 Monofilament absorbable synthetic sutures - other
Device class
Class III
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 MONOFILAMENT ABSORBABLE SYNTHETIC SUTURES.

Other devices from Aptos, LLC

See all devices from Aptos, LLC →

Properties

  • Supplied sterile
  • Sterilise before use
  • Implantable
Other properties (9, all answered No)