activL®
Part of a family of 6 devices: see the family page
Ref FW919P
activL® (FW919P) is a Class I device made by Aesculap AG, registered in EUDAMED on 19 Jan 2026 (Basic UDI-DI 40392390000006812P), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number40392390000006812P 04046963151348 | Date19 Jan 2026 | StatusActive |
Official records
- EUDAMED public site 40392390000006812P
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- Withdrawn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
- ACTIV L tray plastic
- Model / reference
- FW919P
- Primary DI / UDI-DI
- 04046963151348
- Basic UDI-DI
- 40392390000006812P
- EMDN code
- S010401 Trays, baskets, tubs for sterilisation and their components
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005504
Similar devices in this category
Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.
- KHEIRON PC0030 by S.M.A.I.O
- PST Corp. 7000S by Plastic Sterilizing Tray Corporation
- PST Corp. 2600B by Plastic Sterilizing Tray Corporation
- GAP ENDO-EXO MEDULLARY SYSTEM GAP-INE200 by Orthopediatrics Canada ULC
- The Simple Locking Intra Medullary System PEG-CEM-24 by ORTHOPEDIATRICS CANADA ULC
- The Fassier-Duval Telescopic IM System FD-PEG-CEM-28 by ORTHOPEDIATRICS CANADA ULC
- Stryker Universal Select Sterilization Tray System by Paragon Medical Inc.