Steriway
by Levent Tıbbi Cihazlar Baharat ve Şifa Bitkileri İthalat ihracat Anonim Şirketleri 322 variants
Ref STWTP120300
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 | Number8680904SH3 08680904003059 | Date11 May 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- Withdrawn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 Products
- Model / Reference
- STWTP120300
- Primary DI / UDI-DI
- 08680904003059
- Basic UDI-DI
- 8680904SH3
- Direct Marketing DI
- 08680904003059
- EMDN Code
- S01010201 Flat sterilisation pouches, tyvek/plastic film
- Device Class
- Class I
- EU market of registration
- Romania
Manufacturer details
- EUDAMED SRN
- TR-MF-000054014
Other devices from Levent Tıbbi Cihazlar Baharat ve Şifa Bitkileri İthalat ihracat Anonim Şirketleri
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