7,315 results · 55ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

NeutrArt

FDA registration
ASSET MEDIKAL TASARIM SAN. TIC. A.S.·2 products·🇹🇷 Türkiye

GTK Disposable Needle Guides

FDA registration
GEOTEK MEDIKAL VE SAGLIK HIZ. LTD. STI·1 product·🇹🇷 Türkiye

ONAPGO Pump

FDA registration
CANE' S.p.A.·1 product·🇮🇹 Italy

Z-MOTION SYSTEM: Z-TABLE

FDA registration
CONTROL-X MEDICAL, Zrt.·1 product·🇭🇺 Hungary

MILLENSYS Vision Tools Workspace "PACS/VNA"

FDA registration
MILLENSYS·1 product·🇪🇬 Egypt

heat it

FDA registration
Kamedi GmbH·1 product·🇩🇪 Germany

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·Blazer (II, II HTD, Primie HTD)

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·Blazer II HTD / Blazer Prime HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·Blazer II HTD, Blazer Prime HTD

PTH (Parathyroid) Intact ELISA

FDA UDI
DRG International Inc·00840239036452·The PTH (Parathyroid) Intact ELISA is intended ...

Intact-PTH [Parathyroid Hormone] ELISA [Enzyme-Linked ImmunoSorbent Assay]

FDA UDI
BIOMERICA, INC.·00083059070224·The Biomerica Intact-PTH ELISA is intended for ...

PTH (Intact, 1-84) ELISA

FDA UDI
AMERICAN LABORATORY PRODUCTS COMPANY, LTD.·B24221IPTHUE010·The PTH (Intact, 1-84) ELISA is intended for us...

Intact-PTH [Parathyroid Hormone] ELISA [Enzyme-Linked ImmunoSorbent Assay]

FDA UDI
BIOMERICA, INC.·08305900070224·The Biomerica Intact-PTH ELISA is intended for ...

PTH (Parathyroid) Intact ELISA

FDA UDI
DRG Instruments Gesellschaft mit beschränkter Haftung·04048474036459·The PTH (Parathyroid) Intact ELISA is intended ...

Scantibodies Laboratory, Inc.

FDA UDI
SCANTIBODIES LABORATORY, INC.·00850002253115·Whole PTH (1-84) Specific IRMA (Coated Bead)

ST AIA-PACK Intact PTH

FDA UDI
TOSOH CORPORATION·14560189210445·

ECG Cable/Leadwires

FDA 510(k)
FDA Class 2 ·Cardiovascular

Oximeter

FDA 510(k)
FDA Class 2 ·Cardiovascular

Access Total βhCG (5th IS) (reagent pack)

Device
EU IVDD · Eu Ivd Annex 2 List B ·Beckman Coulter Inc.·On the market·32 countries

Automated External Defibrillators (Non-Wearable)

FDA Pre-Market Approval
FDA Class 3 ·Zoll R Series