Steri̇cont
by Stericont Sterilizasyon ve Tıbbi Aletler Tic. A.Ş. 319 variants
Ref S220.13Model STERİCONT
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8684474SSC000015C 08684474000685 | Date20 Feb 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Sterilization Container
- Model / Reference
- STERİCONT, S220.13
- Primary DI / UDI-DI
- 08684474000685
- Basic UDI-DI
- 8684474SSC000015C
- Direct Marketing DI
- 08684474000685
- EMDN Code
- S010499 Sterilisation containers - other
- Device Class
- Class I
- Market of Registration
- Austria
Manufacturer details
- EUDAMED SRN
- TR-MF-000041489
Other devices from Stericont Sterilizasyon ve Tıbbi Aletler Tic. A.Ş.
See all devices from Stericont Sterilizasyon ve Tıbbi Aletler Tic. A.Ş. →
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No