50 results · 22ms · Sources: EU EUDAMED, US FDA

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Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH IV UNIPOLAR PULSE GENERATOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CYBERLITH

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950022427·CALIPER CASTROVIEJO LONG BEAK STRAIGHT 0-40MM 6...

TLX

FDA UDI
Nuvasive, Inc.·00887517729484·TLX Alignment Tool

WorkMate™ Unity™

FDA UDI
ST. JUDE MEDICAL, INC.·05415067047168·Module Software Upgrade Single License

Trimline

FDA UDI
ORMCO CORPORATION·00889989051230·UPPER LEFT FIRST MOLAR TRIMLINE BAND SIZE 19

Rampart O

FDA UDI
SPINEOLOGY INC.·M7402800019·15x30mm Trial

BK-1544 BE OK SCOOP DISK

FDA 510(k)
FDA Class 1 ·Physical Medicine

Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay

FDA Pre-Market Approval
FDA Class 3 ·VENTANA MMR RxDx Panel