| Primary Device ID | 54953170465203 |
| NIH Device Record Key | a1c27c09-5e86-42d5-b90c-606c8250f99a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VISIGLIDE2 |
| Version Model Number | G-260-3545S |
| Catalog Number | N5368231 |
| Company DUNS | 690543319 |
| Company Name | TERUMO CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4500 Millimeter |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 8. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04953170465208 [Primary] |
| GS1 | 54953170465203 [Package] Contains: 04953170465208 Package: [5 Units] In Commercial Distribution |
| OCY | Endoscopic guidewire, gastroenterology-urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-22 |
| Device Publish Date | 2025-07-14 |
| 54953170358260 | VISIGLIDE2 Single Use Guidewire |
| 54953170358253 | VISIGLIDE2 Single Use Guidewire |
| 54953170358246 | VISIGLIDE2 Single Use Guidewire |
| 54953170358239 | VISIGLIDE2 Single Use Guidewire |
| 54953170358222 | VISIGLIDE2 Single Use Guidewire |
| 54953170358215 | VISIGLIDE2 Single Use Guidewire |
| 54953170358208 | VISIGLIDE2 Single Use Guidewire |
| 54953170358154 | VISIGLIDE2 Single Use Guidewire |
| 54953170465203 | VISIGLIDE2 Single Use Guidewire |
| 54953170465197 | VISIGLIDE2 Single Use Guidewire |
| 54953170465180 | VISIGLIDE2 Single Use Guidewire |
| 54953170465173 | VISIGLIDE2 Single Use Guidewire |
| 54953170465166 | VISIGLIDE2 Single Use Guidewire |
| 54953170465159 | VISIGLIDE2 Single Use Guidewire |
| 54953170465142 | VISIGLIDE2 Single Use Guidewire |
| 54953170465135 | VISIGLIDE2 Single Use Guidewire |