| Primary Device ID | 10628341930168 |
| NIH Device Record Key | 9b29c493-e7b0-4b4c-8800-1a4d5fc9d4f5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vacuum Lock |
| Version Model Number | 1 |
| Catalog Number | VB |
| Company DUNS | 206950904 |
| Company Name | CDR Systems Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00628341930161 [Primary] |
| GS1 | 10628341930168 [Package] Contains: 00628341930161 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 | 2020-01-08 |
| Device Publish Date | 2019-12-31 |
| 10628341930410 - Solid Bolus | 2025-01-29 Solid Bolus |
| 10628341930526 - Extremity Lock | 2025-01-29 Extremity Board (MR SAFE) |
| 10628341930519 - Extremity Lock | 2024-12-19 Extremity Board |
| 10628341930502 - EQUILIBRIUM | 2024-02-02 EQUILIBRIUM Rotating Overlay System |
| 10628341930373 - Thermoplastic | 2024-01-08 Thermoplastic Immobilization Materials |
| 10628341930380 - Thermoplastic | 2024-01-08 Thermoplastic Immobilization Mask |
| 10628341930465 - TBI | 2023-03-16 TBI Positioning System With Spoiler |
| 10628341930441 - Freedom | 2023-03-03 Freedom S-Type Overlay |