AccessGUDID - DEVICE: IPPS Overlay (00841439102138)

GUDID

Device Identifier (DI) Information

Brand Name: IPPS Overlay
Version or Model: 20IL430135
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 20IL430135
Company Name: MEDTEC, INC.

Primary DI Number: 00841439102138
Issuing Agency: GS1
Commercial Distribution End Date: March 12, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 103977526 *Terms of Use

Device Description: Reusable non-sterile foot panel for use with Calypso 4D Localization System and Siemens ZXT or TXT base

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?
40897	Indexed-immobilization patient positioning system	A assembly of devices used primarily in radiation therapy applications, and consisting of an indexed treatment or imaging table (couch) that contains locking interfaces used to attach various positioning and immobilization devices to numbered or lettered (indexing) points on the table. It is used to ensure both adequate positioning and immobilization of a patient and to help ensure reproducible alignment between a target portion of the patient's anatomy and the radiation beams or fields used in radiation therapy treatments, diagnostic imaging studies. It may accommodate a variety of anatomically targeted patient positioning and immobilization attachments.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IXQ	Table, radiographic, stationary top

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K973842	000

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
Length: 110 Centimeter

Device Record Status

Public Device Record Key: 46ca7b4b-a627-4f5d-9df9-cdf967c4e65b
Public Version Date: August 11, 2022
Public Version Number: 6
DI Record Publish Date: August 02, 2017