AccessGUDID - DEVICE: ZA KIT, T IN FT, URETHANE, 35"X84" (00840828162548)

GUDID

Device Identifier (DI) Information

Brand Name: ZA KIT, T IN FT, URETHANE, 35"X84"
Version or Model: MCZ-3584FP
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 9268
Company Name: CURBELL MEDICAL PRODUCTS, INC.

Primary DI Number: 00840828162548
Issuing Agency: GS1
Commercial Distribution End Date: January 08, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 796452311 *Terms of Use

Device Description: ZA KIT, T IN FT, URETHANE, 35"X84"

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?
36063	Stretcher mattress	A large, flat, cushion or pad with a strong cover filled with a resilient material (e.g., foam rubber) designed to be used on a stretcher to provide patient comfort whilst they lie upon it. It is much thinner than a bed mattress and is placed on top of, and typically secured to, the stretcher support platform covering this area. This is a general-purpose device that has no special therapeutic purpose.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FPP	Stretcher, Hand-Carried

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: c1f1cd7b-4ae1-4933-b4c0-037727d39339
Public Version Date: January 09, 2019
Public Version Number: 2
DI Record Publish Date: September 24, 2018