Extremity Lock EB-24STD-K

GUDID 10628341930526

Extremity Board (MR SAFE)

CDR Systems Inc

Indexed-immobilization patient positioning system
Primary Device ID10628341930526
NIH Device Record Keyca639372-ea6b-432c-ad26-c4de9a540d26
Commercial Distribution StatusIn Commercial Distribution
Brand NameExtremity Lock
Version Model Number1
Catalog NumberEB-24STD-K
Company DUNS206950904
Company NameCDR Systems Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca
Phone403-850-7035
Emailinfo@cdrsys.ca

Device Identifiers

Device Issuing AgencyDevice ID
GS100628341930529 [Primary]
GS110628341930526 [Package]
Contains: 00628341930529
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYEAccelerator, Linear, Medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-29
Device Publish Date2025-01-21

On-Brand Devices [Extremity Lock]

10628341930519Extremity Board
10628341930526Extremity Board (MR SAFE)

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