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Results for “Turbocast”

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Registry EUDAMED 418 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 418

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Netherlands 418

Risk class Class I 418 Class IIa Class IIb Class III Class II (US)

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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418 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Turbocast UDI-DI 08717973153399

Ttape Company,Netherlands

Active Regimes: CE MDR Registry: EUDAMED Class:I
329 variants
- Turbocast 0813
- Turbocast 1613
- Turbocast 1620
- Turbocast 3033
- Turbocast 3060/9
- Turbocast 4061/9
- Turbocast RE1601NS
- Turbocast RE1612
- Turbocast RE2503
- Turbocast RE2504
- Turbocast RE2520/9NS
- Turbocast RE2552
- Turbocast RE3000/9
- Turbocast RE3004/NS
- Turbocast RE3023/NS
- Turbocast RE4024NS
- See all variants of this device
Turbocast Ortho (NS) UDI-DI 08717973151975

Ttape Company,Netherlands

Active Regimes: CE MDR Registry: EUDAMED Class:I
87 variants
- Turbocast Ortho (NS) OS253
- Turbocast Ortho (NS) OS320/9
- See all variants of this device

Showing 341-360 of 418

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