AccessGUDID - DEVICE: NA (10810030861543)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: MCM440
Commercial Distribution Status: In Commercial Distribution
Catalog Number: MCM440
Company Name: MID CENTRAL MEDICAL CORP.

Primary DI Number: 10810030861543
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 076907973 *Terms of Use

Device Description: Underpad Mount Armboard. This armboard is designed to slide under the OR Table, stretcher, or imaging table pad and be held in place by the weight of the patient. Can be adjusted as needed. Phenolic material is completely radiolucent for C-arm capabilities. Exposed Armboard portion is 6"W x 24"L. .

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?
42308	Operating table orthopaedic extension, non-powered	A non-powered, orthopaedic device intended to function as a freestanding framework or that can be attached to an operating table or table top to provide additional support to a patient's body segment or part during orthopaedic surgical procedures (e.g., lower trunk for traction of the legs, upper body during shoulder or spinal surgery, C- or O-arm use). It typically consists of height, length and angle adjustable supports or telescopic bars/plates (e.g., leg spar).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NOD	Board, Arm (With Cover), Non-Sterile

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
Length: 39 Inch
Width: 17 Inch
Height: 0.375 Inch

Device Record Status

Public Device Record Key: cc357926-e7ef-40e8-ac9e-4bd490fe84a4
Public Version Date: February 06, 2025
Public Version Number: 4
DI Record Publish Date: September 30, 2020