2,650 results
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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
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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