MAILL'TUB
FR-MF-000000921 · France · PORT-BRILLET
MAILL'TUB is registered in the European database on medical devices as a manufacturer, with 111 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 111 |
|---|
Most frequent device types declared: STOCKINETTE to be incorporated in PROCEDURE PACKS, TUBULAR STOCKINETTE JERSEY to be used as protective apparel.
Devices declared under this manufacturer
- Caleçon coton Adulte petit
- JERSEY TUBULAIRE COTON ECRU 5cm x 25m
- Maillot coton Adulte petit
- STOCKINETTE ROULEE 1/1 COTON ECRU 10x130
- STOCKINETTE ROULEE 1/1 COTON ECRU 10x200
- STOCKINETTE ROULEE 1/1 COTON ECRU 15x190 M4
- STOCKINETTE ROULEE COTON ECRU 10x150
- STOCKINETTE ROULEE COTON ECRU 15x100
- STOCKINETTE ROULEE COTON ECRU 15x200
- STOCKINETTE ROULEE COTON ECRU 20x200
- STOCKINETTE ROULEE JERSEY COTON ECRU 10x100
- STOCKINETTE ROULEE NON COUSUE 1/1 COTON ECRU 15x190
Showing 12 of 111 declared devices.
Catalogue references include A1013002C11, A1020002C11, A1510002C21, A1520002C21, A1523002C11NS, A2016002C11NS.
European nomenclature codes declared: T0306, M03050201, M03050202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 111 |
| 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 | 111 |
|---|---|
| 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. MAILL'TUB was not found in either the U.S. or the Canadian register.