| Primary Device ID | 54987350727126 |
| NIH Device Record Key | 18400431-8222-4038-8d21-ae4709504f93 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VENOJECT |
| Version Model Number | XX*MN2000TE |
| Company DUNS | 690543319 |
| Company Name | TERUMO CORPORATION |
| Device Count | 100 |
| 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(800)283-7866 |
| tmccustomer.admin@terumomedical.com | |
| Phone | +1(800)283-7866 |
| tmccustomer.admin@terumomedical.com |
| Special Storage Condition, Specify | Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Do not store at extreme temperature and humidity. Avoid direct sunlight. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04987350727121 [Unit of Use] |
| GS1 | 34987350727122 [Primary] |
| GS1 | 54987350727126 [Package] Contains: 34987350727122 Package: [30 Units] In Commercial Distribution |
| JKA | Tubes, vials, systems, serum separators, blood collection |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2016-09-09 |
| 04987350740601 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 04987350740625 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 04987350740649 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 54987350740668 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 04987350740687 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 54987350740699 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 04987350740700 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
| 04987350745422 - GLIDEWIRE GT-R | 2026-02-16 Glidewire GT-R Guide Wire |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VENOJECT 72460010 0998267 Live/Registered |
KABUSHIKI KAISHA JINTAN TERUMO 1973-06-12 |
![]() VENOJECT 72315927 0885119 Dead/Expired |
JINTAN TERUMO CO., LTD. 1969-01-06 |