320 P37,SY,BE,2L,2LD,BE(3&9),6FT,STKR 25893

GUDID 00840828180399

320 P37,SY,BE,2L,2LD,BE(3&9),6FT,STKR

CURBELL MEDICAL PRODUCTS, INC.

Electrical mains power extension cable
Primary Device ID00840828180399
NIH Device Record Keyd555356c-5dd7-4d4a-b883-d63f96e27134
Commercial Distribution StatusIn Commercial Distribution
Brand Name320 P37,SY,BE,2L,2LD,BE(3&9),6FT,STKR
Version Model Number3001-991-644
Catalog Number25893
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
GS100840828180399 [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

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00840828195942 - GEN4 INTERACTIVE2026-02-13 GEN4 INTERACTIVE
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