| Primary Device ID | EBGO615501 |
| NIH Device Record Key | 3a0b279d-8e07-45e9-b262-d19872a5a80c |
| Commercial Distribution Discontinuation | 2017-05-18 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | BegoPal+ |
| Version Model Number | 61550 |
| Catalog Number | 61550 |
| Company DUNS | 316483072 |
| Company Name | BEGO Bremer Goldschlägerei Wilh. Herbst GmbH & Co.KG |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +4942120280 |
| info@bego.com |
| Special Storage Condition, Specify | Between 0 and 0 *Dry |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EBGO615501 [Primary] |
| EJH | Alloy, Metal, Base |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-04-26 |
| Device Publish Date | 2016-11-15 |
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