Solid Bolus S-Bolus

GUDID 10628341930410

Solid Bolus

CDR Systems Inc

Patient positioning thermoplastic mould material
Primary Device ID10628341930410
NIH Device Record Key9a0bad69-1e86-45f6-9558-1d04a174534b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSolid Bolus
Version Model Number1
Catalog NumberS-Bolus
Company DUNS206950904
Company NameCDR Systems Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 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
GS100628341930413 [Primary]
GS110628341930410 [Package]
Contains: 00628341930413
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 [Solid Bolus]

00628341930406Solid Bolus
10628341930410Solid Bolus

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