3701 P37,1TO1,2FT,STKR 25896

GUDID 00840828180405

3701 P37,1TO1,2FT,STKR

CURBELL MEDICAL PRODUCTS, INC.

Electrical mains power extension cable
Primary Device ID00840828180405
NIH Device Record Key01f4c826-ac43-4b2b-96e4-0beb181e01c3
Commercial Distribution StatusIn Commercial Distribution
Brand Name3701 P37,1TO1,2FT,STKR
Version Model Number3001-991-647
Catalog Number25896
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100840828180405 [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 Date2026-02-02
Device Publish Date2020-05-20

On-Brand Devices [3701 P37,1TO1,2FT,STKR]

008408281811983701 P37,1TO1,2FT,STKR
008408281804123701 P37,1TO1,2FT,STKR
008408281804053701 P37,1TO1,2FT,STKR

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