| Primary Device ID | 07640130434592 |
| NIH Device Record Key | 94fe0ef9-e3a3-4fca-ac57-9d88fbd0bbb7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Passeo-35 |
| Version Model Number | 4/120/130 |
| Catalog Number | 383277 |
| Company DUNS | 480862817 |
| Company Name | Biotronik 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 | 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 | +1(888)345-0374 |
| jon.brumbaugh@biotronik.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
| Storage Environment Temperature | Between 10 Degrees Celsius and 40 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight Store in a dry location |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07640130434592 [Primary] |
| LIT | Catheter, angioplasty, peripheral, transluminal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |