Azoto Dm Sico
by SICO Società Italiana Carburo Ossigeno S.p.A. 55 variants
Ref DMAZOXXRD01B00400ZNZ
Expiring
CE MDR
Valid until
13 Jun 2027
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number805948259N201EV 08059482590884 | Date14 May 2026 | StatusActive |
Certificates
- EPT 0477.MDR.22/4850.2 Expiring
Quality management system EU MDR
- Certifier
- Eurofins Product Testing Italy S.r.l. 0477
- Issued
- 7 Apr 2026
- Expires
- 13 Jun 2027
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device Name
- Azoto Dm Sico
- Model / Reference
- DMAZOXXRD01B00400ZNZ
- Primary DI / UDI-DI
- 08059482590884
- Basic UDI-DI
- 805948259N201EV
- Direct Marketing DI
- 08059482590846
- EMDN Code
- V0902 Clinical/therapeutic applications liquid nitrogen
- Device Class
- Class IIa
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000028343
Other devices from SICO Società Italiana Carburo Ossigeno S.p.A.
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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