Aseltech
by Asel Tibbi Aletler A.S. 1,000+ variants
Ref CN-5233Model ASELTECH
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8681376ASELTECH201529AX 08681376091452 | Date21 Dec 2023 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Sterilization Container Systems
- Model / reference
- ASELTECH, CN-5233
- Primary DI / UDI-DI
- 08681376091452
- Basic UDI-DI
- 8681376ASELTECH201529AX
- EMDN code
- S010401 Trays, baskets, tubs for sterilisation and their components
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000019723
Overview
AI-generated summary, 10 Nov 2026
ASELTECH is a sterilization container system, as indicated by its device type name. It is listed under EU MDR registration with Class I status, model ASELTECH, and reference CN-5233.
Other devices from Asel Tibbi Aletler A.S.
Properties
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