Network®
by Network Medical Products Limited 23 variants
Ref ES 9090 PLUS 20Model Sterile Single Use Precision LASIK Blade for the use with Nidek MK-2000 Microkeratome Plus 20
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-05056100702233 05056100702233 | Date8 Jun 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- NETWORK® Precision LASIK Blade
- Model / Reference
- Sterile Single Use Precision LASIK Blade for the use with Nidek MK-2000 Microkeratome Plus 20, ES 9090 PLUS 20
- Primary DI / UDI-DI
- 05056100702233
- Basic UDI-DI
- B-05056100702233
- EMDN Code
- Z1212020585 Microkeratomy instruments - consumables
- Device Class
- Class IIa
- EU market of registration
- Malta
Manufacturer details
- EUDAMED SRN
- GB-MF-000025518
- Authorised representative
- Advena Limited MT-AR-000000234
Other devices from Network Medical Products, Ltd.
Properties
Other properties (10)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No