Primary Device ID | 10628341930526 |
NIH Device Record Key | ca639372-ea6b-432c-ad26-c4de9a540d26 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Extremity Lock |
Version Model Number | 1 |
Catalog Number | EB-24STD-K |
Company DUNS | 206950904 |
Company Name | CDR Systems Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca | |
Phone | 403-850-7035 |
info@cdrsys.ca |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00628341930529 [Primary] |
GS1 | 10628341930526 [Package] Contains: 00628341930529 Package: [1 Units] In Commercial Distribution |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-01-29 |
Device Publish Date | 2025-01-21 |
10628341930519 | Extremity Board |
10628341930526 | Extremity Board (MR SAFE) |