airlock® ACC1022P0003
by Novastep
Ref ACC1022P0003
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number370087950TF1X0203000LD | Date3 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03700879517810 | Date18 Jun 2026 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- airlock®
- Generic Name
- Device sterilization/disinfection container, reusable
- Device Name
- Accessories for cleaning and holding devices
- Model / Ref / Catalog
- ACC1022P0003
- Primary DI / UDI-DI
- 03700879517810
- Basic UDI-DI
- 370087950TF1X0203000LD
- Direct Marketing DI
- 03700879517810
- FDA Product Code
- FSM
- EMDN Code
- L091099 Osteosynthesis instruments, reusable - other
- GMDN Term
- Device sterilization/disinfection container, reusable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Market of Registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Novastep
Properties
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: 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
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Lot / Batch Number: No
- Expiration Date: No