| Primary Device ID | 08435510679767 |
| NIH Device Record Key | 5f027bbf-98ea-431d-9efb-360c2e899769 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TITANIUM VAC REG |
| Version Model Number | CONT/INT CM*DM |
| Catalog Number | 5349313 |
| Company DUNS | 462032145 |
| Company Name | HERSILL SL |
| 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 | false |
| Lot Batch | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08435510679767 [Primary] |
| KDP | Regulator, Vacuum |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-01-15 |
| Device Publish Date | 2026-01-07 |
| 08435510680053 | VACUSILL 3 REG MEDIUM VACUUM + DH WALL CONNECTION + SAFETY TRAP |
| 08435510680046 | VACUSILL 3 REG LOW VACUUM + DH WALL CONNECTION + SAFETY TRAP |
| 08435510680039 | VACUSILL 3 REG PEDIATRIC CONTINUOUS INTERMITTENT + DH WALL CONNECTION + SAFETY TRAP |
| 08435510679873 | VACUSILL 3 REG CONTINUOUS INTERMITTENT + DH WALL CONNECTION + LG PATIENT PORT |
| 08435510679866 | VACUSILL 3 REG CONTINUOUS INTERMITTENT + PM WALL CONNECTION + LG PATIENT PORT |
| 08435510679774 | VACUSILL 3 REG CONTINUOUS INTERMITTENT + OM WALL CONNECTION + SAFETY TRAP |
| 08435510679767 | VACUSILL 3 REG CONTINUOUS INTERMITTENT + CM WALL CONNECTION + DM PATIENT PORT |
| 08435510679101 | VACUSILL 3 REG CONTINUOUS INTERMITTENT + DH WALL CONNECTION + SAFETY TRAP |