Home GUDID 07630039101404
DUOLITH®
Primary DI 07630039101404
Brand DUOLITH®
Company Storz Medical AG
Model SD1 Tower
Catalog number 19880.0005
Device description The device is indicated for extracorporeal shock wave treatment.
Published 2021-06-29
Public version status New
Distribution status In Commercial Distribution
MRI safety MR Unsafe
Rx true Product Codes# Code, Name table Code Name ISA Massager, Therapeutic, Electric NBN Generator, Shock-Wave, For Pain Relief PZL Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ISA Massager, Therapeutic, Electric Physical Medicine 1 NBN Generator, Shock-Wave, For Pain Relief Unknown 3 PZL Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers General, Plastic Surgery 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07630039101404 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07630039101404 07630039101404 7630039101404
GMDN Terms# Term, Definition table Term Definition Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system An assembly of devices designed to provide electromechanical orthopaedic extracorporeal shock wave therapy (OEST) and pneumatic pressure wave therapy to treat musculoskeletal disorders. It is typically mobile and includes a control unit that uses both an electrical current and compressed air to create kinetic energy which is transferred to a patient's body upon contact (e.g., with two different hand-held surface applicators) to produce mechanical shock waves at selected amplitudes and frequencies. It is used to treat soft-tissue pain and inflammation near bones, disorders such as tendinopathies and lateral/medial epicondylitis, and to stimulate osteogenesis.
Regulatory Flags# DUNS number 481967776 Device count 1 Serial number true Manufacturing date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00850071298017 Smart-RST Hyperion Medical Technologies, Inc. ISA 2026-06-02 16973368290059 Medisana Zhangzhou Easepal Medical Science And Technology Co., Ltd. ISA 2026-04-30 07630039101855 MASTERPULS® Storz Medical AG ISA 2026-04-15 00045915831424 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831431 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831448 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831455 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831462 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831479 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831486 Human Touch Human Touch, LLC ISA 2026-01-12 00045915831493 Human Touch Human Touch, LLC ISA 2026-01-12 08034108512679 Plus Handpiece DEKA M.E.L.A. SRL ISA 2025-10-22 00197344153605 MEDLINE MEDLINE INDUSTRIES, INC. ISA 2025-10-17 08800205600003 Neuclare Deepsonbio Co., Ltd ISA 2025-08-08 08809643652087 CERAGEM Master V9 CERAGEM Co., Ltd. ISA 2025-07-15 00810140061355 RENPHO Joicom Corporation ISA 2024-11-19 00810140061362 RENPHO Joicom Corporation ISA 2024-11-19 00810140061379 RENPHO Joicom Corporation ISA 2024-11-19 00810140061386 RENPHO Joicom Corporation ISA 2024-11-19 00810140061393 RENPHO Joicom Corporation ISA 2024-11-19 00810140061409 RENPHO Joicom Corporation ISA 2024-11-19 00810140061416 RENPHO Joicom Corporation ISA 2024-11-19 00810140061447 RENPHO Joicom Corporation ISA 2024-11-19 00810140061690 RENPHO Joicom Corporation ISA 2024-11-19 00810140061706 RENPHO Joicom Corporation ISA 2024-11-19 00810140061768 RENPHO Joicom Corporation ISA 2024-11-19 00810140061782 RENPHO Joicom Corporation ISA 2024-11-19 00810140061799 RENPHO Joicom Corporation ISA 2024-11-19 00810140061805 RENPHO Joicom Corporation ISA 2024-11-19 00810140061812 RENPHO Joicom Corporation ISA 2024-11-19