Manufacturer
Blink Device
United StatesLegal entities : Blink Device Company
Markets : Austria · Italy · United States
Approvals : EU – class I, IIa · United States (FDA) – 510(k) : 2 · class II · latest in 2020 · see on the FDA website
EU representative : AF Pharma Service Europe SL (Spain)
- On the market
- No longer marketed
- 93/42 Former directive, not yet certified under the MDR
- Click a category to see competitors, a model to open its EUDAMED record.
| Category | EMDN code | Registered models | Class | Contact |
|---|---|---|---|---|
| Neuromuscular stimulation equipment - consumables | Z12062885 | I MDR | EUDAMED record Report an error | |
| Neuromuscular stimulation equipment - other | Z12062899 | IIa MDR | EUDAMED record Report an error |
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