87 results
·
44ms
·
Sources: EU EUDAMED, US FDA
Reprieve by Regenesis
FDA registration
REGENESIS BIOMEDICAL, INC.·1 product·🇺🇸 United States
Reprieve by RegenesisTM
FDA 510(k)
FDA Class 2
·Physical Medicine
Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
FDA classification
FDA Class 2
·Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
DIGITAL RADIOGRAPHY E1
FDA registration
Canon.Inc·1 product·🇯🇵 Japan
manometer, cuff, cuff bladder, inflation bulb and optioned
FDA registration
ORANTECH INC.·2 products·🇨🇳 China
DIGITAL RADIOGRAPHY E1
FDA registration
CANON INC.·1 product·🇯🇵 Japan
DIGITAL RADIOGRAPHY E1
FDA registration
CANON COMPONENTS, INC.·1 product·🇯🇵 Japan
Match-complete set
FDA registration
MedSource Labs, LLC·2 products·🇺🇸 United States
Aneroid Sphygmomanometer
FDA registration
WENZHOU CARETEK MEDICAL DEVICE CO., LTD·2 products·🇨🇳 China
Aneroid Sphygmomanometer
FDA registration
WUXI EXANOVO MEDICAL INSTRUMENT CO., LTD.·2 products·🇨🇳 China
VariAx
FDA UDI
Stryker Trauma SA·37613153067994·LOCKING SCREWS, CROSS-PIN
ASO Ankle Stabilizer, Universal
FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357236206·
GFAP Reagent Kit (Alinity i, LN 04W1722)
FDA registration
ABBOTT IRELAND·1 product·🇮🇪 Ireland
GFAP Reagent Kit (Alinity i, LN 04W1722)
FDA registration
ABBOTT LABORATORIES·1 product·🇺🇸 United States
GFAP Reagent Kit (Alinity i, LN 04W1722)
FDA registration
ABBOTT GmbH·1 product·🇩🇪 Germany
Software, non contact, optical camera-based measurement of pulse rate
FDA registration
FACEHEART CORP.·1 product·🇹🇼 Taiwan
Aneroid Sphygmomanometer
FDA 510(k)
FDA Class 2
·Cardiovascular
FILMARRAY RESPIRATORY PANEL (RP)
FDA 510(k)
FDA Class 2
·Microbiology
Votion
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730009708·Votion™ Mini .022 LR7 NC SBT -10T 0A 0O DB (10PK)
Votion
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730009548·Votion™ .022 LR6 NC SBT -20T 0A 0DDO DB (10PK)