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Aptos

by Aptos LLC 5 variants

Ref DRN031, LLS019, LLSS020, EVS003, AT2G027, SRN032, NS7018, AS023, LLT2G012, EV001, LLT2GS013, LLNMB017, LLTMB014, EVHA002, AT2GS028, LLN2GSSP010, EB005, AW2.0033, IEM008Model Body DRN N, Light Lift Spring Method, Light Lift Spring Method S, Visage Excellence Method S, Light Lift Thread Method N, Sole Rhinoplasty N, Nano Spring Method, Light Lift Spring Method N, Light Lift Thread Method, Visage Excellence Method, Light Lift Thread Method S, Light Lift Needle Method B, Light Lift Thread Method B, Visage Excellence Method HA, Light Lift Thread Method N S, Sole Rhinoplasty, Body Excellence Method, Body Wire Method 2/0, Intimate Excellence Method

Aptos (DRN031) is a device classified as Class IIb, Class III and Class IIa in the EU made by Aptos, LLC, registered in EUDAMED on 29 Jan 2026 (Basic UDI-DI B-4860120240085), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-4860120240085 Basic UDI-DI Date29 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  • Withdrawn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 - Non Absorbable Surgical Sutures
Aptos Threads - Absorbable Surgical Sutures
Apos Threads - Absorbable Surgical Sutures
Aptos Instruments
Model / reference
Body DRN N, DRN031, Light Lift Spring Method, LLS019, Light Lift Spring Method S, LLSS020, Visage Excellence Method S, EVS003, Light Lift Thread Method N, AT2G027, Sole Rhinoplasty N, SRN032, Nano Spring Method, NS7018, Light Lift Spring Method N, AS023, Light Lift Thread Method, LLT2G012, Visage Excellence Method, EV001, Light Lift Thread Method S, LLT2GS013, Light Lift Needle Method B, LLNMB017, Light Lift Thread Method B, LLTMB014, Visage Excellence Method HA, EVHA002, Light Lift Thread Method N S, AT2GS028, Sole Rhinoplasty, LLN2GSSP010, Body Excellence Method, EB005, Body Wire Method 2/0, AW2.0033, Intimate Excellence Method, IEM008
Primary DI / UDI-DI
4860120240085, 4860120240177, 4860120240252, 4860120240207, 4860120240030, 4860120240139, 4860120240221, 4860120240054, 4860120240153, 4680120240191, 4860120240245, 4860120240306, 4860120240290, 4860120240313, 4860120240047, 4860120240276, 4860120240214, 4860120240092, 4860120240368
Basic UDI-DI
B-4860120240085, B-4860120240177, B-4860120240252, B-4860120240207, B-4860120240030, B-4860120240139, B-4860120240221, B-4860120240054, B-4860120240153, B-4680120240191, B-4860120240245, B-4860120240306, B-4860120240290, B-4860120240313, B-4860120240047, B-4860120240276, B-4860120240214, B-4860120240092, B-4860120240368
EMDN code
H010201010401, H0101010199, H010201010404, H010202020101
Device class
Class IIb
Class III
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

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Properties

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