AccessGUDID - DEVICE: BodyFIX (04056719000202)

GUDID

Device Identifier (DI) Information

Brand Name: BodyFIX
Version or Model: P10102-227
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: P10102-227
Company Name: 3C-Medical Intelligence GmbH

Primary DI Number: 04056719000202
Issuing Agency: GS1
Commercial Distribution End Date: July 16, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 314546664 *Terms of Use

Device Description: The BodyFIX Localizer features three Localizer screens specially designed for stereotactic application. Each of these Localizer screens has three slots with special plastic tubes already inserted. As an alternative to the plastic tubes, these BodyFIX® 14 Localizer Fiducial Set Aluminium contrast rods allow improved visualization in CT.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
40895	Vacuum-mould patient positioning system	An 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).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IYE	Accelerator, Linear, Medical

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 84888bce-09c0-453a-a360-da2b21f65b01
Public Version Date: December 15, 2023
Public Version Number: 5
DI Record Publish Date: August 23, 2016