NUNC A/S
DK-MF-000024621 · Denmark · Roskilde
NUNC A/S is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 5 |
|---|
Among these devices, 15 are declared sterile.
Devices declared under this manufacturer
- Nunc™ CryoTube, 1,0 mL, internal thread, Green Band, PP/PP, sterile
- Nunc™ CryoTube, 1,0mL, sterile, internal thread, foot, conical
- Nunc™ CryoTube, 1,0mL, sterile, internal thread, starfoot, conical
- Nunc™ CryoTube, 1,8mL, sterile, internal thread, round
- Nunc™ CryoTube, 1,8mL, sterile, internal thread, starfoot, round
- Nunc™ CryoTube, 1.8mL, sterile, internal thread, round
- Nunc™ CryoTube, 3,6mL, sterile, internal thread, round
- Nunc™ CryoTube, 3,6mL, sterile, internal thread, starfoot, round
- Nunc™ CryoTube, 4,5mL, sterile, internal thread, starfoot, round
- Nunc™ CryoTube, 4.5mL, sterile, internal thread, round
- Nunc™ IVF Dish Non-treated 35mm
- Nunc™ IVF Dish Non-treated 60mm
Showing 12 of 15 declared devices.
Catalogue references include 150270, 179830, 363401, 366524, 366656, 377267.
European nomenclature codes declared: W050299, U080206.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | NUNC A/S (DK) · FDA 3003150158 |
| Devices in EUDAMED | 15 |
| Country of registration | Denmark |
Device-level evidence
| Devices with a numeric GTIN | 15 |
|---|---|
| Found in the U.S. device database | 15 |
| Share | 100.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | NUNC A/S |
North American profile: Both markets. NUNC A/S is registered in both the United States and Canada.