| Primary Device ID | 00884838074286 |
| NIH Device Record Key | 6a16bf2b-de2f-4a4b-9d5d-7de1dc1f5e5e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Portable DR Panel Protector |
| Version Model Number | 9890-010-88161 |
| Catalog Number | 712031 |
| Company DUNS | 314101218 |
| Company Name | Philips Medical Systems DMC GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | true |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884838074286 [Primary] |
| KXJ | Table, radiologic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2016-09-19 |
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