i-Dixel

Primary DI
04548213026784
Brand
i-Dixel
Company
J.MORITA MFG.CORP.
Model
i-Dixel
Published
2017-02-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
LLZSystem, Image Processing, Radiological

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LLZSystem, Image Processing, RadiologicalRadiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K073704000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K073704000I-DIXELJ. Morita USA, Inc.2008-02-21LLZ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04548213026784PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04548213026784045482130267844548213026784

GMDN Terms#

Term, Definition table
TermDefinition
Basic x-ray clinical assessment support softwareA software program intended to display, analyse/process, and possibly acquire static two-dimensional (2-D) x-ray images of bones and/or the abdominothoracic region, acquired by a basic diagnostic x-ray system, to support a healthcare provider with clinical assessment (e.g., diagnosis, triage, image quality assessment) of a trauma or condition (typically orthopaedic, cardiac or pulmonary). It is not dedicated to treatment planning and does not incorporate adaptive/dynamic machine learning (ML) models.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Handling Environment Atmospheric Pressure00
Handling Environment Humidity00
Handling Environment Temperature00
Storage Environment Atmospheric Pressure00
Storage Environment Humidity00
Storage Environment Temperature00

Regulatory Flags#

DUNS number
693811465
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04548213024698i-Dixeli-Dixel2016-09-23
04548213024704i-Dixeli-Dixel2016-09-23
04548213024711i-Dixeli-Dixel2016-09-23
04548213024728i-Dixeli-Dixel2016-09-23
04548213024735i-Dixeli-Dixel2016-09-23
04548213025176i-Dixeli-Dixel2016-09-09
04548213025183i-Dixeli-Dixel2016-09-23
04548213025282i-Dixeli-Dixel2016-09-23
04548213025299i-Dixeli-Dixel2016-09-23
04548213026760i-Dixeli-Dixel2017-02-12
04548213026777i-Dixeli-Dixel2017-02-12
04548213026791i-Dixeli-Dixel2017-02-12
04548213026807i-Dixeli-Dixel2017-02-12
04548213026814i-Dixeli-Dixel2017-02-12
04548213026821i-Dixeli-Dixel2017-02-12
04548213026838i-Dixeli-Dixel2017-02-12
04548213026845i-Dixeli-Dixel2017-02-12
04548213026852i-Dixeli-Dixel2017-02-12
04548213026944i-Dixeli-Dixel2017-02-12
04548213026951i-Dixeli-Dixel2017-02-12

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Primary DI, Brand, Company table
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TKRL0001FF640PointCloud Knee InstrumentsUnik Orthopedics Inc.LLZ2026-10-20
TKRL0001FLI00PointCloud Knee InstrumentsUnik Orthopedics Inc.LLZ2026-10-20
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TKRL0001L0LD0PointCloud Knee InstrumentsUnik Orthopedics Inc.LLZ2026-10-20
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