419 P37,GE,2LD,STKR 26357

GUDID 00840828181648

419 P37,GE,2LD,STKR

CURBELL MEDICAL PRODUCTS, INC.

Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable Electrical mains power extension cable
Primary Device ID00840828181648
NIH Device Record Keye6b9b5e8-3eec-49fa-8630-441bcddd93e5
Commercial Distribution StatusIn Commercial Distribution
Brand Name419 P37,GE,2LD,STKR
Version Model Number521209900404
Catalog Number26357
Company DUNS796452311
Company NameCURBELL MEDICAL PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com
Phone1-800-235-7500
Emailmwinter@curbell.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]
GS100840828181648 [Primary]

FDA Product Code

ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered
ILQSystem, Communication, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-15
Device Publish Date2020-10-07

On-Brand Devices [419 P37,GE,2LD,STKR]

00840828100366419 P37,GE,2LD,STKR
00840828181303419 P37,GE,2LD,STKR
00840828181648419 P37,GE,2LD,STKR

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