Skip to content

Aseltech

by Asel Tibbi Aletler A.S. 1,000+ variants

Ref BP-1302Model ASELTECH

Aseltech (BP-1302) is a Class I device made by Asel Tibbi Aletler A.S., registered in EUDAMED on 17 Jan 2024 (Basic UDI-DI 8681376ASELTECH201530AG), active as of 24 Oct 2026.

Active European Union

CE MDR

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8681376ASELTECH201530AG Basic UDI-DI 08681376066375UDI-DIDate17 Jan 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Scraper
Model / reference
ASELTECH, BP-1302
Primary DI / UDI-DI
08681376066375
Basic UDI-DI
8681376ASELTECH201530AG
EMDN code
L1703 Ophthalmology curettes, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019723

Related devices

Category: Ophthalmic curette, reusable

Similar devices in this category

Other devices filed under OPHTHALMOLOGY INSTRUMENTS, REUSABLE.

Other devices from Asel Tibbi Aletler A.S.

See all devices from Asel Tibbi Aletler A.S. →

Properties

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