ΛΑΜΕΝΤ ΙΚΕ
GR-MF-000020993 · Greece · ΜΕΛΙΣΣΙΑ
ΛΑΜΕΝΤ ΙΚΕ is registered in the European database on medical devices as a manufacturer, with 42 devices declared. It has a company name that cannot be normalised for comparison.
What this manufacturer declares
| Class IIa | 42 |
|---|
Most frequent device types declared: LAMED NON STERILE GAUZE SWABS, STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 5cm X 4,5m.
Among these devices, 21 are declared sterile.
Devices declared under this manufacturer
- LAMED
- LAMED 5cm X 5cm 8ply
- STIRIXIS ΑΥΤΟΚΟΛΛΗΤΗ ΓΑΖΑ ΑΠΟΣΤΕΙΡΩΜΕΝΗ 10Χ10CM 50ΤΜΧ
- STIRIXIS ΑΥΤΟΚΟΛΛΗΤΗ ΓΑΖΑ ΑΠΟΣΤΕΙΡΩΜΕΝΗ 10Χ20CM 25ΤΜΧ
- STIRIXIS ΑΥΤΟΚΟΛΛΗΤΗ ΓΑΖΑ ΑΠΟΣΤΕΙΡΩΜΕΝΗ 10Χ25CM 10ΤΜΧ
- STIRIXIS ΑΥΤΟΚΟΛΛΗΤΗ ΓΑΖΑ ΑΠΟΣΤΕΙΡΩΜΕΝΗ 8Χ10CM 50ΤΜΧ
- STIRIXIS ΓΑΖΑ ΑΠΟΣΤΕΙΡΩΜΕΝΗ 36Χ40CM 10ΤΕΜ
- STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 10cm X 4,5m
- STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 12cm X 4,5m
- STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 15cm X 4,5m
- STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 20cm X 4,5m
- STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 5cm X 4,5m
Showing 12 of 42 declared devices.
Catalogue references include 5200250220196, 5200250220202, 5200250220677, 5213012320041, 5213012320072, 5213012320133.
European nomenclature codes declared: M030499, M0201020101, M04010101, M0202010102, M0201020202, M0201020102.
United States market access
| FDA establishment register | Name not comparable |
|---|---|
| Devices in EUDAMED | 42 |
| Country of registration | Greece |
Device-level evidence
| Devices with a numeric GTIN | 42 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |