AccessGUDID - DEVICE: Ritter (00841709111587)

GUDID

Device Identifier (DI) Information

Brand Name: Ritter
Version or Model: 9A337001-866
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 9A337001-866
Company Name: MIDMARK CORPORATION

Primary DI Number: 00841709111587
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 005036025 *Terms of Use

Device Description: The Ritter 24" UltraFree wide foot rest, Dark Linen colored, is designed to provide added support under the patient's feet.

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):	No
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?
37048	Footrest	A device intended to be used to sustain/retain a patient's foot or feet in a desired position. This device will often be considered an accessory to one or more parent devices. It is typically constructed of metal/plastic/rubber and can be attached to, e.g., operating tables/examination tables/treatment chairs.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GBB	CHAIR, SURGICAL, AC-POWERED

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: 08111e15-36d6-4dd7-a8b0-e43269062b8a
Public Version Date: May 15, 2020
Public Version Number: 1
DI Record Publish Date: May 07, 2020