CROSSER® GEN200
GUDID 00801741067617
CROSSER® Generator
Bard Peripheral Vascular, Inc.
Mechanical atherectomy system generator, electrical output Mechanical atherectomy system generator, electrical output| Primary Device ID | 00801741067617 |
| NIH Device Record Key | c0969c0f-36cd-47dc-bea3-6ef156e8f0bf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CROSSER® |
| Version Model Number | GEN200 |
| Catalog Number | GEN200 |
| Company DUNS | 135057938 |
| Company Name | Bard Peripheral Vascular, Inc. |
| 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 | true |
| 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 |
Customer Support Contacts
| Phone | +1(800)321-4254 |
| medical.services@crbard.com | |
| Phone | +1(800)321-4254 |
| medical.services@crbard.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741067617 [Primary] |
FDA Product Code
| PDU | Catheter for crossing total occlusions |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-09-24 |
| Device Publish Date | 2016-09-13 |
On-Brand Devices [CROSSER®]
| 00801741067617 | CROSSER® Generator |
| 00801741067471 | CROSSER® System Foot Switch |
Trademark Results [CROSSER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CROSSER 98376113 not registered Live/Pending |
Future Full-Screen Tong Intelligent Technology Group Co., Ltd. 2024-01-25 |
 CROSSER 88154952 5894604 Live/Registered |
Crosser Technologies AB 2018-10-15 |
 CROSSER 85387982 4170527 Live/Registered |
Flowcardia, Inc. 2011-08-03 |
 CROSSER 79262277 not registered Live/Pending |
"VELOSIPED" LTD 2019-04-09 |
 CROSSER 76656589 3313198 Live/Registered |
Flowcardia, Inc. 2006-03-14 |
 CROSSER 76018684 not registered Dead/Abandoned |
L&R Industries Inc. 2000-04-05 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.