| Primary Device ID | 00884838076006 | 
| NIH Device Record Key | 1cdf21de-be0c-440b-ad89-170f51cd7da4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | MRC 200 0508 ROT 1003 PREOWNED | 
| Version Model Number | 9890-000-30021 | 
| Catalog Number | 9890-000-30021 | 
| Company DUNS | 314101218 | 
| Company Name | Philips Medical Systems DMC GmbH | 
| Device Count | 1 | 
| DM Exempt | true | 
| 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 | false | 
| 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 | false | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00884838076006 [Primary] | 
| ITY | Assembly, tube housing, x-ray, diagnostic | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-02-11 | 
| Device Publish Date | 2019-01-11 | 
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