FDA.reportPublic FDA data

BodyFIX

Primary DI
04056719001728
Brand
BodyFIX
Company
3C-Medical Intelligence GmbH
Model
P10102-305
Catalog number
P10102-305
Device description
BodyFIX® Hygienic Drape Manifold Tube (2x15000mm) is used to cover the manifold tube for hygienic purposes.
Published
2016-08-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
IYEAccelerator, Linear, Medical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
IYEAccelerator, Linear, MedicalRadiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K121530000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K121530000BODYFIX SYSTEMMedical Intelligence Medizintechnik GmbH2012-06-20IYE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04056719000264PackageGS15In Commercial Distribution
04056719001728PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04056719000264040567190002644056719000264
04056719001728040567190017284056719001728

GMDN Terms#

Term, Definition table
TermDefinition
Vacuum-mould patient positioning systemAn assembly of devices designed to apply a vacuum to a cushion or bag filled with foam-like material that is placed under, on, or around a patients body parts. A vacuum is applied to the contents of the cushion forming a patient specific (custom-made) mould. The moulds can be whole body or selected body parts and help ensure adequate positioning and immobilization of the patient during diagnostic imaging and/or radiation therapy procedures facilitating reproducible positioning for serial procedures. This system typically includes reusable foam-filled bags, cushions, a vacuum unit, hardware, seals, and interfaces used to connect the mould to another patient positioning system (PPS).

Regulatory Flags#

DUNS number
314546664
Device count
1
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04056719002268iGUIDEP10603-111-224P10603-1112026-04-22
04056719002190iGUIDEP10603-111-223P10603-1112019-08-01
04056719001704iGUIDEP10603-109P10603-1092016-08-23
04056719001742iGUIDEP10603-110P10603-1102017-02-24
04056719002039iGUIDEP10603-111P10603-1112017-10-13
04056719001735BodyFIXP10102-309P10102-3092016-08-23
04056719001773FraxionP10106-322 P10106-322 2016-08-23
04056719001780FraxionP10106-323 P10106-323 2016-08-23
04056719001803HeadFIXP10103-309 P10103-309 2016-08-23
04056719001810HeadFIXP10103-311 P10103-311 2016-08-23
04056719001827HeadFIXP10103-312 P10103-312 2016-08-23
04056719001834HeadFIXP10103-403 P10103-403 2016-08-23
04056719001858HeadFIXP10103-603 P10103-603 2016-08-23
04056719001865HeadFIXP10103-604 P10103-604 2016-08-23
04056719002220iBEAM®P10105-1822020-06-18
04056719002251iBEAMP10105-184P10105-1842022-07-12
04056719002244HexaPODP10603-300P10603-3002021-09-28
04056719002213iBEAM®P10105-3002020-08-20
04056719002237iBEAM®P10105-1832020-07-07
04056719000011BodyFIXP10102-101 P10102-101 2016-08-23

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Primary DI, Brand, Company table
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