HANDLES, LIGHT, SURGICAL, STEOILE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SURGICAL LIGHT 22 SERIES

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SYNTHES LIGHT GUIDE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SURGICAL LIGHT - CHALLENGE 22 SERIES

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ACULUX, MODEL AX3001, AX3002

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3

FDA 510(k)

FDA Class 1 ·Microbiology

VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT

FDA 510(k)

FDA Class 1 ·Microbiology

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·Enitra 8 HF-T, Edora 8 HF-T QP, Edora 8 HF-T, Enitra 8 HF-T QP, Evity 8 HF-T, Evity 8 HF-T QP

Novocastra

FDA UDI

LEICA BIOSYSTEMS NEWCASTLE LTD·05055331333896·NCL-L-KAP-581-U is intended for the qualitative...

PATIENT EXAMINATION GLOVES

FDA 510(k)

FDA Class 1 ·General Hospital

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·Edora 8 HF-T QP 407137, Edora 8 HF-T 407138, Evity 8 HF-T QP 407139, Evity 8 HF-T 407140, Enitra 8 HF-T QP 407141, Enitr

Seat Ergometer ergoselect 100 K BP, SpO2

FDA UDI

ergoline GmbH·04059358000343·

Defibrillator, Implantable, Dual-Chamber

FDA Pre-Market Approval

FDA Class 3 ·Ilivia Neo 7 HF -T QP, Ilivia Neo 7 HF -T, Intica Neo 7 HF -T QP, Intica Neo 7 HF -T, Intica Neo 5 HF -T QP, Intica Neo

Keenhealth

FDA UDI

Sevenground Trading B.V.·08719699632622·K-BP-568digital blood pressure monitor for home...

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·Edora, Evity, Enitra, Enticos 8 HF-T/ QP

Keenhealth

FDA UDI

Sevenground Trading B.V.·08719699632615·K-BP-119 digital blood pressure monitor for hom...

FDA Pre-Market Approval

600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS

FDA Pre-Market Approval

600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS

TRANSPARENT ANESTHESIA FILTER

FDA 510(k)

FDA Class 2 ·Anesthesiology

PARTNER INFUSION SYSTEM:

FDA 510(k)

FDA Class 2 ·General Hospital