Becton Dickinson, S.A.
ES-MF-000016479 · Spain · San Agustin del Guadalix
Becton Dickinson, S.A. is registered in the European database on medical devices as a manufacturer, with 169 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 169 |
|---|
Among these devices, 138 are declared sterile, 82 with a measuring function.
Devices declared under this manufacturer
- DISCARDIT
- Eclipse
- Eclipse Luer-Lok
- Eclipse SmartSlip
- Emerald
- MICROLANCE
- Not Applicable
- Plastipak
- Plastipak Luer-Lok
- SOLOSHOT
- SafetyGlide
Showing 12 of 169 declared devices.
Catalogue references include 300847, 303262, 305787, 305959, 307725, 307753.
European nomenclature codes declared: A0101010101, A020102010201, A0101010102, A020102010202, A020102010101, A020102020102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BECTON DICKINSON, S.A. (ES) · FDA 3002682307 |
| Devices in EUDAMED | 169 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 169 |
|---|---|
| Found in the U.S. device database | 34 |
| Share | 20.1 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | BECTON DICKINSON |
⚠️ A similar name exists; unverified — why.