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)