CRYOPAL
FR-MF-000003522 · France · BUSSY SAINT GEORGES
CRYOPAL is registered in the European database on medical devices as a manufacturer, with 271 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 271 |
|---|
Most frequent device types declared: ARPEGE - SERENY T, ARPEGE-CRYOMEMO, CRYOMEMO, ESPACE - SERENY T, FREELOX PORTABLE.
Among these devices, 201 are declared active.
Devices declared under this manufacturer
- ARPEGE140 Liquide - CryoMemo Temperature - Niveau - Régulation - sorti
- ARPEGE170SB-L-2
- ARPEGE75SB-L-2
- ESP151SB-LC-2
- ESPACE331 Liquide non caréné - Plateau tournant - CryoMemo Temperature
- FREELOX 2 RESERVE 44L US HUL
- FREELOX 3 PESON 1.2L CE IT
- GT21 avec 6 canisters 1 Etage Inox
- GT9 avec 6 canisters 1 Etage Inox
- GT9 sans équipement
- Kit upgrade ARP140 Liq - ITNR-RS/420+MEMO+KD
- Kit upgrade ARP55-75 - ITNR-RS/420+MEMO+KD
Showing 12 of 271 declared devices.
Catalogue references include ACC-UPBOX40-1, ACC-UPBOX5575-2, ENS-ESP661-69-61, ESP151SB-LC-2, GT 9, LF 107301.
European nomenclature codes declared: V0499,V92, V92, V0499, Z12159099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 271 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 271 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. CRYOPAL was not found in either the U.S. or the Canadian register.