| Primary Device ID | 00859273007038 |
| NIH Device Record Key | b7250ec4-c5b5-45b6-87d2-cb85da799b0a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Veriflow™ |
| Version Model Number | R-10003 |
| Catalog Number | R-10003 |
| Company DUNS | 080031617 |
| Company Name | RELIGN CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00859273007038 [Primary] |
| GS1 | 08592730070030 [Previous] |
| GS1 | 10859273007035 [Package] Package: Shipper [6 Units] In Commercial Distribution |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-28 |
| Device Publish Date | 2020-02-20 |
| 08592730070030 | Fluid management accessory disposable |
| 00859273007038 | Fluid management accessory disposable |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VERIFLOW 88136804 not registered Live/Pending |
Relign Corporation 2018-09-28 |
![]() VERIFLOW 87178648 not registered Dead/Abandoned |
Watlow Electric Manufacturing Company 2016-09-21 |
![]() VERIFLOW 85720681 4419696 Live/Registered |
Invisible Sentinel, Inc. 2012-09-05 |