CALL CORD,PERMALIGHT,SGL,JERON 790,8PD,WHITE,7FT

GUDID B4849953P70

CALL CORD,PERMALIGHT,SGL,JERON 790,8PD,WHITE,7FT

Crest Healthcare Supply

Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button Ambulatory call button
Primary Device IDB4849953P70
NIH Device Record Keyeb754c01-4b4f-4be5-9b73-6da118a27e6e
Commercial Distribution StatusIn Commercial Distribution
Brand NameCALL CORD,PERMALIGHT,SGL,JERON 790,8PD,WHITE,7FT
Version Model Number9953YZZ
Company DUNS151772415
Company NameCrest Healthcare Supply
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
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

Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com
Phone1-320-275-3382
Emailcustomerservice@cresthealthcare.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB4849953P70 [Primary]

FDA Product Code

IQASystem, Environmental Control, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-08
Device Publish Date2023-10-31

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