AccessGUDID - DEVICE: MedSource Stretcher (00816703029848)

GUDID

Device Identifier (DI) Information

Brand Name: MedSource Stretcher
Version or Model: MS-EFS124-BL
Commercial Distribution Status: In Commercial Distribution
Catalog Number: Not Applicable
Company Name: MEDSOURCE INTERNATIONAL LLC

Primary DI Number: 00816703029848
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 041674552 *Terms of Use

Device Description: Folding Stretcher (2 Legs,2 Wheels) Blue

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?
35843	Ambulance stretcher, manual	A manually-operated device consisting of a platform mounted on a wheeled frame designed for use by emergency medical services (EMS) primarily to facilitate easy transport of a recumbent patient to and from ambulance vehicles (e.g., automobiles, aeroplanes, helicopters, boats); it does not include a powered or powered-assisted lifting mechanism. It is typically constructed of lightweight materials and has an undercarriage that opens and folds when it is removed from or pushed into the ambulance; it also usually includes locking devices that match with the locking/docking devices in the ambulance.	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: d7c5f0b5-1762-4046-ade8-ad717b01f965
Public Version Date: August 09, 2021
Public Version Number: 1
DI Record Publish Date: July 30, 2021