AccessGUDID - DEVICE: JUMPER,72",P103 INL TO P102 90,MOLDED (00840828185448)

GUDID

Device Identifier (DI) Information

Brand Name: JUMPER,72",P103 INL TO P102 90,MOLDED
Version or Model: JU72-858
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 27336
Company Name: CURBELL MEDICAL PRODUCTS, INC.

Primary DI Number: 00840828185448
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 796452311 *Terms of Use

Device Description: JUMPER,72",P103 INLINE TO P102 90 DEG,MOLDED,T-T,R-B,B-B

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: 5c1519b7-2e1d-4dbc-8ac6-6e948954e0d4
Public Version Date: January 31, 2022
Public Version Number: 1
DI Record Publish Date: January 21, 2022