| Primary Device ID | 20357515032595 |
| NIH Device Record Key | 52ade093-19e4-4c2e-acc5-638d76d3fb2d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UltiCare |
| Version Model Number | 03259 |
| Company DUNS | 024723541 |
| Company Name | ULTIMED, 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 | 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10357515032598 [Primary] |
| GS1 | 20357515032595 [Package] Contains: 10357515032598 Package: Box [100 Units] In Commercial Distribution |
| GS1 | 30357515032592 [Package] Package: [5 Units] In Commercial Distribution |
| GS1 | 40357515032599 [Package] Contains: 30357515032592 Package: [4 Units] In Commercial Distribution |
| FMF | Syringe, Piston |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2025-06-24 |
| Device Publish Date | 2016-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTICARE 75476846 2253550 Live/Registered |
UltiMed Inc. 1998-04-27 |
![]() ULTICARE 74523307 not registered Dead/Abandoned |
MEDICRAT INC. 1994-05-02 |
![]() ULTICARE 73477381 1351431 Dead/Cancelled |
HEALTH DATA SCIENCES CORPORATION 1984-04-26 |