Vertetrac

Primary DI
07290015711104
Brand
Vertetrac
Company
MEDITRAC LTD.
Model
VERT9
Device description
The Vertetrac provides safe, simple, compact, and effective treatment of lumbar spine disorders and brings to both the patient and physician a means of powerful, dynamic traction with simultaneous, three-dimensional action without the need for traction beds or restrictive braces. Thus, the Vertetrac allows the patient maximum mobility with minimal restrictions or discomfort during treatment. The Vertetrac facilitates the treatment of the patient by the health service professional while also allowing chronic sufferers to administer self-treatment under qualified medical supervision.
Published
2022-07-25
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
IQEOrthosis, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
IQEOrthosis, LumbarPhysical Medicine1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
17290015711101PackageGS11In Commercial Distribution
37290015711105PackageGS13In Commercial Distribution
07290015711104PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1729001571110117290015711101
3729001571110537290015711105
07290015711104072900157111047290015711104

GMDN Terms#

Term, Definition table
TermDefinition
Wearable lumbar spine traction deviceAn externally-worn orthopaedic device designed to apply traction to the lumbar spine to relieve symptoms of back pain and sciatica. It consists of adjustable components worn superiorly under the rib cage, and inferiorly over the iliac crests, with rods holding the components apart that can be adjusted to apply traction forces by separation. It may include an additional attachable component intended for the treatment of scoliosis. It is intended for use in the home or a clinical setting. This is a reusable device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
514587369
Device count
1
Premarket exempt
true
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07290015711203Cervico2000CERV82022-07-25
07290015711302D.B.S. Dynamic Brace SystemDBS12022-07-25

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Primary DI, Brand, Company table
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