| Primary Device ID | 00818016020239 |
| NIH Device Record Key | ed91ece0-3316-433a-acea-76eb194c48fe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | United Urologics Closed System Catheter Kit |
| Version Model Number | UU12RK |
| Company DUNS | 080428707 |
| Company Name | UNITED UROLOGICS 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 | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00818016020239 [Primary] |
| GS1 | 10818016020236 [Package] Package: [100 Units] In Commercial Distribution |
| KOD | Catheter, Urological |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-03-22 |
| 00818016020307 | UU16CK |
| 00818016020291 | UU14CK |
| 00818016020284 | UU12CK |
| 00818016020277 | UU14SK |
| 00818016020260 | UU12SK |
| 00818016020253 | UU16RK |
| 00818016020246 | UU14RK |
| 00818016020239 | UU12RK |
| 00818016020222 | UU18K |
| 00818016020215 | UU16K |
| 00818016020208 | UU14K |
| 00818016020185 | UU10K |
| 00818016020178 | UU08K |
| 00818016020161 | UU06K |
| 00818016020017 | UU06 |