Multiplus
by Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇. 5 variants
Ref AL UG30Model 5000 ml
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 | Number868078904027ALG50105264R 08680789040279 | Date28 Apr 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- Withdrawn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
- Ultrasound Gel
- Model / Reference
- 5000 ml, AL UG30
- Primary DI / UDI-DI
- 08680789040279
- Basic UDI-DI
- 868078904027ALG50105264R
- EMDN Code
- Z11040185 Ultrasound scanners - consumables
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000045198
Other devices from Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇.
See all devices from Alg İlaç Sanayi̇ Ti̇caret Ltd. Şti̇. →
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