| Primary Device ID | 04250435532133 |
| NIH Device Record Key | 3bcfa560-2777-4fbc-bee3-a03a956aa26e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DORO LUCENT iXI Transfer-Collision Indicator |
| Version Model Number | 4003.513 |
| Company DUNS | 313517922 |
| Company Name | pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04250435532133 [Primary] |
| HBL | Holder, Head, Neurosurgical (Skull Clamp) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-25 |
| Device Publish Date | 2019-01-25 |
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