| Primary Device ID | 04056481005481 |
| NIH Device Record Key | 80b476d7-b6b3-45fa-bda0-6429261de600 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Calibration Insert Spinal Probe 3.62Mm |
| Version Model Number | 53520 |
| Catalog Number | 53520 |
| Company DUNS | 314482980 |
| Company Name | Brainlab AG |
| Device Count | 1 |
| DM Exempt | false |
| 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 | 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 |
| Phone | +49899915680 |
| contact@brainlab.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04056481005481 [Primary] |
| HAW | Neurological Stereotaxic Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04056481005481]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-15 |
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