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Aysam

by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi 1,000+ variants

Ref A6074060

Aysam (A6074060) is a Class IIb device made by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi, registered in EUDAMED on 18 Mar 2024 (Basic UDI-DI B-08698823363468), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08698823363468 Basic UDI-DI Date18 Mar 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
16 Mm Yi̇vli̇ Kanüllü Vİda Ti̇tanyum (16 Mm Threaded Cannulated Screw Titanium) 4,5 X 60 Mm
A6074060
Model / reference
A6074060
Primary DI / UDI-DI
08698823363468, 08698823388850
Basic UDI-DI
B-08698823363468, B-08698823388850
EMDN code
P09120603 Cannulated screws
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000017437

Similar devices in this category

Other devices filed under CANNULATED SCREWS.

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Properties

  • Sterilise before use
  • Implantable
Other properties (12, all answered No)