EndoSize
by Therenva France EUDAMED510(k)
Ref EndoSize v3.2.x510(k) K160376
Product code LLZEMDN Z12040192
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number376026248EndoSizeD4 | Date5 Feb 2026 | StatusActive |
| United States | FDA 510(k)SESE 510(k) | NumberK160376 | Date12 Apr 2016 | StatusActive |
Coverage
- Active
- Not covered
- United States
- European Union
Specification
- Model / Reference
- EndoSize v3.2.x
- Primary DI / UDI-DI
- 37602624800154
- Basic UDI-DI
- 376026248EndoSizeD4
- Direct Marketing DI
- 37602624800154
- 510(k) Number
- FDA Product Code
- LLZ
- EMDN Code
- Z12040192 General medicine diagnosis and monitoring instruments - medical device software
- Device Class
- Class IIa EUDAMEDClass II 510(k)
- Regulation
- 21 CFR Part 892.2050
- Special Device Type
- Software
- Market of Registration
- France
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent
Truth per registry
| Field | EUDAMED | 510(k) |
|---|---|---|
| Device Class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- FR-MF-000000343
Other devices from Therenva Sas
Properties & raw data
Show properties, registry sources and raw records
Other properties (12)
- 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
- Incorporates Medicinal Product: No
Sources (2)
- EUDAMED 8ab32d36-4c11-4205-ba62-4f13b9ab08b9
- FDA 510(k) K160376