BA KIT,WE,P37(90),6',BE,P37,INL,1',STKR 26501

GUDID 00840828182164

BA KIT,WE,P37(90),6',BE,P37,INL,1',STKR

CURBELL MEDICAL PRODUCTS, INC.

Electrical mains power extension cable
Primary Device ID00840828182164
NIH Device Record Key7233764e-859b-4836-a2c5-737c21b11183
Commercial Distribution StatusIn Commercial Distribution
Brand NameBA KIT,WE,P37(90),6',BE,P37,INL,1',STKR
Version Model Number300909910609
Catalog Number26501
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100840828182164 [Primary]

FDA Product Code

FNLBed, Ac-Powered Adjustable Hospital

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2026-01-29
Device Publish Date2020-11-10