2,650 results · 90ms · Sources: EU EUDAMED, US FDA

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·PHOTOTOME(TM) SYSTEM 2700

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·YAGMASTER ND:YAG OP LASER

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·HORIZON(TM) YAG LASER MODEL 2000

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·LASAG TOPAZ ND:YAG LASER SYSTEM

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

FDA Pre-Market Approval
FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

PHOTOSILK PLUS PULSED LIGHT SYSTEM AND LASER ATTACHMENT

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

EASYRA ALKALINE PHOSPHATASE, ASPARTATE AMINOTRANSFERASE AND AMYLASE REAGENTS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·BRYAN (TM) CERVICAL DISC

Percutaneously Delivered Prostheses And Tricuspid Valves

FDA Pre-Market Approval
FDA Class 3 ·Edwards EVOQUE Tricuspid Valve Replacement System

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·PRESTIGE: LP(TM) CERVICAL DISC

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MERIDIAN AND DISCOVERY PACEMAKER SYSTEMS

OMNIMAX S4

FDA UDI
SharpLight Technologies Ltd.·07290110240042·The Dermatologic Treatment Systems (DTS) device...

Amylase

Basic UDI-DI
EU IVDD · Eu Ivd General ·C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.·1 device

Amylase

Basic UDI-DI
EU IVDD · Eu Ivd General ·NS BIOTEC·1 device

SILHOUETTE(TM) IC OR SILHOUETTE(TM) & LASER-LOK (TM)

FDA 510(k)
FDA Class 2 ·Dental

Stellar M22 for Intense Pulsed Light (IPL) and Laser System

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ACE ALKALINE PHOSPHATASE REAGENT, AMYLASE REAGENT, ALT REAGENT, AST REAGENT

FDA 510(k)
FDA Class 2 ·Clinical Chemistry