Pega Medical Inc.

Pega Medical Inc.

Pega Medical specializes in the design, evaluation,
manufacturing, and regulatory submission of medical devices and
surgical instruments. Services include conceptual and detail
design bioengineering (Computer Aided Design, Finite Element
Modeling and Analysis, 3-D modeling), ergonomic and industrial
design, mechanical testing, contract manufacturing, forensic
bioengineering, US-FDA, TPP-Canada and Mercosur regulatory
submissions and commercial contacts, TPS, HA and RBM coatings.
Vast experience in Orthopedic and Dental fields.

Company Details

Year Established: 1994

Company Information

Robert Carrire
Title: Director
Area of Responsibility: Domestic Sales & Marketing
Telephone: (514) 322-8560
Fax: (514) 328-9548
Email: Click Here

Ariel R. Dujovne
Title: President
Area of Responsibility: Management Executive
Telephone: (514) 322-8560
Fax: (514) 328-9548
Email: Click Here

Products

Surgical Instruments, Reusable Nes

Endosseous Implants

R&d Medical Devices

Spins (shriner's Pediatric Intramedullary Nail)
A telescopic Nail intended for the treatment of diaphyseal fractures of long bones in pediatric patients, especially used in the treatment of Osteogenesis Imperfecta

Bone Mill For Autologous Htr
Bone mill to generate autologous bone particles for Hard Tissue Reconstruction for Craneo-Maxillofacial, Dental and Orthopaedic Surgery

Biocoat Ha And Plasma Coatings
Distributor for Canada and South America of BIOCOAT's Hidroxilapatite and Plasma Sprayed Titanium Powder for non- cemented fixation of endosseous implants.

Services

Regulatory Mechanical Testing

Bioengineering Consulting Development of surgical instruments and implantable medical devices in the areas of Orthopaedics, Craneo-Maxillofacial and Dentistry. Industrial Design, Ergonomics, Finite Element Analysis, CAD, Rapid and traditional Prototyping, etc.

Supplier Of Components For Eom's

Expert Testimony On Med. Dev. Failure Retrieval analysis of medical devices. Identification and failure analysis of ex-vivo medical device specimens. Currently working as expert technical witness in breast implant litigation.

Prototyping And Mass Production

Regulatory Submissions (fda, Tpp, Anmat) Regulatory submission for medical devices with the US-Food and Drug Administration, Canadian Therapeutic Product Programme and SouthAmerican Regulatory Bodies.

Commercial Contacts Liaison between European, North American and SouthAmerican Medical Device Companies searching for distributors and new products lines.