Linnea

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Rini Ergoteknik AB·1 device

Zeus The Bionic Hand

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Aether Biomedical Spółka z ograniczoną odpowiedzialnością·1 device

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval

FDA Class 3 ·NAVISTAR RMT DS CATHETER

D3 Ultra Duet DFA Respiratory Virus

FDA registration

Ortho-Clinical Diagnostics, Inc.·5 products·🇺🇸 United States

Utility Scissor

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Expert International·1 device

NES Nederland B.V.

Importer

🇳🇱 Netherlands

Novanta Europe GmbH

Authorized representative

🇩🇪 Germany·1 Manufacturer

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330851·L-DFA Influenza A/Influenza B Reagent

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330752·D3 FASTPOINT RESP VIRUS ID KIT

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330776·D3 FASTPOINT LDFA VIR IDKIT BX

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330875·L-DFA Parainfluenza Virus/Adenovirus Reagent

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330769·D3 FASTPOINT LDFA VIR IDKIT BX

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330868·L-DFA RSV/MPV Reagent

D3 Fastpoint

FDA UDI

DIAGNOSTIC HYBRIDS, INC.·30014613330844·Re-Suspension Buffer

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval

FDA Class 3 ·HELIOS II ABLATION CATHETER

NRS Healthcare

Authorized representative

1 Manufacturer·2 Devices

RQS Wojciech Roman

Authorized representative

🇵🇱 Poland·4 Manufacturers

Ldt, Approved By Nys Clep

FDA classification

FDA Not Classified ·Ldt, Approved By Nys Clep

Rheumatoid Factor (RA)

Basic UDI-DI

EU IVDD · Eu Ivd General ·NS BIOTEC·1 device

Glucose

Basic UDI-DI

EU IVDD · Eu Ivd General ·NS BIOTEC·1 device