MEDISTOCK
FR-MF-000007667 · France · CORBAS
MEDISTOCK is registered in the European database on medical devices as a manufacturer, with 367 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 367 |
|---|
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- Aloecare
- Bande crêpe 20cm x 5m / 120 rlx
- Charlotte Clip Non Tissé Bleu
- Embout intra-oraux jaune / 15
- Embout mélangeur pour AUTOMIX - Jaune / 20x50
- Gaine de Stérilisation 250x200 / 2 rlx
- Gaine de stérilisation 250mmx100m avec soufflet/2
- Micros applicateurs fin Bleu / 4800
- PE PLAST STERIBLUE
- PINSON MEDICAL SOLUTION GLOVES NITRILE
- ROULEAUX SALIVAIRES SEPTALINE N°2
- Sur-Chaussures anti-dérapantes Vert Anis
Showing 12 of 367 declared devices.
Catalogue references include 69MC45B, 69SC40BPE, E5006, E5007, K50031B, M15005-5.
European nomenclature codes declared: T01020204, A0280, T010201, T0202, T020604, T0207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 367 |
| 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 | 367 |
|---|---|
| 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. MEDISTOCK was not found in either the U.S. or the Canadian register.