| Primary Device ID | 04052838011488 |
| NIH Device Record Key | 87838d33-957c-4a1d-b9ce-0945cbff0ba5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SonoTip® EBUS Pro Flex |
| Version Model Number | GUS-46-18-022 |
| Catalog Number | GUS-46-18-022 |
| Company DUNS | 318130267 |
| Company Name | Medi-Globe GmbH |
| 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 | true |
| 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 | +4980329730 |
| sales@medi-globe.de |
| Needle Gauge | 22 Gauge |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry, keep away from sunlight |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04052838011488 [Package] Contains: 04052838011495 Package: Box [5 Units] In Commercial Distribution |
| GS1 | 04052838011495 [Primary] |
| FCG | Biopsy Needle |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-01-30 |
| 04052838011488 | SonoTip EBUS Pro with Nitinol Needle, Endobronchial Ultrasound Guided TBNA System for Olympus En |
| 04052838011440 | SonoTip EBUS Pro with Nitinol Needle, Endobronchial Ultrasound Guided TBNA System for Pentax End |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SONOTIP 75825744 2474385 Live/Registered |
MEDI-GLOBE GMBH 1999-10-18 |