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
CodeName
ISAMassager, Therapeutic, Electric
NBNGenerator, Shock-Wave, For Pain Relief
PZLExtracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ISAMassager, Therapeutic, ElectricPhysical Medicine1
NBNGenerator, Shock-Wave, For Pain ReliefUnknown3
PZLExtracorporeal Shock Wave Device For Treatment Of Diabetic Foot UlcersGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K173692000
K202112000
P080028001

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K173692000D-Actor 200 Vibration Massage SystemStorz Medical AG2018-04-13ISA
K202112000Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia HandpieceStorz Medical AG2021-02-21PZL
P080028001STORZ MEDICAL DUOLITH SD1 SHOCK WAVE THERAPYStorz Medical AG2016-01-08NBN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07630039101404PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07630039101404076300391014047630039101404

GMDN Terms#

Term, Definition table
TermDefinition
Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy systemAn 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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
481967776
Device count
1
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07630039101855MASTERPULS®icon37000.00022026-04-15
07630039101909MASTERPULS®R-SW10043000.00022026-03-01
07630039100919MODULITH®SLX-F2290002021-04-13
07630039101817MASTERPULS®MP10023232.01042024-10-01
07630039101343DUOLITH®SD1 R-SW19880.00062021-06-01
07630039101169MASTERPULS®ONE2019-09-16
07630039101039D-ACTOR®2002018-05-28
07630039101060D-ACTOR®1002018-10-28
07630039101121D-ACTOR®502018-11-15
07630039101442MODULITH®SLX-F239000.00012025-04-11
07630039101459MODULITH®SLX-F239000.00022025-04-11
07630039101466MODULITH®SLX-F239000.00032025-04-11
07630039100803StorM-Base 2.032016-09-23
07630039100773DUOLITH®SD1 T-Top2016-06-27
07630039101336DUOLITH®SD1 Tower2020-03-23
07630039100230MODULITH®SLX-F22016-08-24
07630039101398DUOLITH®SD1 T-Top21362.01022021-04-08
07630039101350MAGNETOLITH31500.00022021-06-01
07630039101329DUOLITH®SD1 T-Top2020-03-23
07630039101046XR-MX/1000FD43 (80 kW)292552021-04-08

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