| Primary Device ID | 00884838103566 |
| NIH Device Record Key | 2e67a5ab-77c8-42df-b029-3c974343bf73 |
| Commercial Distribution Discontinuation | 2030-11-09 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pinnacle Radiation Therapy Planning System |
| Version Model Number | 18.0 |
| Catalog Number | 45980171803X |
| Company DUNS | 829526560 |
| Company Name | Philips Medical Systems (cleveland), Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| 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 | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com | |
| Phone | +1(800)722-9377 |
| pros.support@philips.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884838103566 [Primary] |
| MUJ | System, planning, radiation therapy treatment |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-08-06 |
| Device Publish Date | 2020-11-09 |
| 00884838103566 | 18.0 |
| 00884838102965 | 16.4 |