Aseltech

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

Ref BM-6902Model ASELTECH

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number8681376ASELTECH201501A9 Basic UDI-DI 08681376056604UDI-DI	Date17 Jan 2024Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name: Separator
Model / reference: ASELTECH, BM-6902

Primary DI / UDI-DI: 08681376056604
Basic UDI-DI: 8681376ASELTECH201501A9
EMDN code: L059001 Vaginal speculums, reusable

Device class: Class I
EU registration type: Standard device
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000019723

Other devices from Asel Tibbi Aletler A.S.

Aseltech

Class I
Aseltech

Class I
Aseltech

Class I
Aseltech

Class I
Aseltech

Class I
Aseltech

Class I

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

Properties

Sterilise before use
Reusable

Other properties (12)

Supplied sterile: No
Implantable: No
Contains latex: No
Reprocessed single-use device: No
Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
Incorporates a substance derived from human blood or plasma: No
Contains human tissues or cells: No
Contains animal tissues or cells: No
Contains endocrine-disrupting substances: No
Administering medicine: No
Measuring function: No
Incorporates a medicinal substance: No