| Primary Device ID | 00884838107403 |
| NIH Device Record Key | f0696e15-9a8e-49f6-9345-f72f491d373a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DA200ULTRA+LMB |
| Version Model Number | 9890-000-87331 |
| Catalog Number | 9890-000-87331 |
| 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 | 00884838107403 [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 | 2023-07-10 |
| Device Publish Date | 2023-06-30 |
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