AccessGUDID - DEVICE: (800,103 P37,RAULAND 800,BED EXIT,2 LIGHTS,22 OHM,CLAMP,MOLDED (00840828174916)

GUDID

Device Identifier (DI) Information

Brand Name: (800,103 P37,RAULAND 800,BED EXIT,2 LIGHTS,22 OHM,CLAMP,MOLDED
Version or Model: 3001-990-931
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 25021
Company Name: CURBELL MEDICAL PRODUCTS, INC.

Primary DI Number: 00840828174916
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 796452311 *Terms of Use

Device Description: 800,103 P37,RAULAND 800,BED EXIT,2 LIGHTS,22 OHM,CLAMP,MOLDED

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?
36092	Electrical mains power extension cable	An insulated electrical cord designed with a mains electricity supply plug at one end and single or multiple outlet socket clusters at the other end, intended to enable a connection between a medical device and a mains electricity supply. It is typically used where there is a need for many electrically-powered medical devices, e.g., in the operating room (OR). It is manufactured to medical grade standards for use in healthcare facilities and the home, providing the required legislative level of electrical safety; it may include an adaptor/transformer. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
ILQ	System, Communication, 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: 539d2c03-9f60-4572-847e-5247d51f6281
Public Version Date: November 27, 2019
Public Version Number: 1
DI Record Publish Date: November 19, 2019