Primary Device ID | 00818016020161 |
NIH Device Record Key | 43a37e29-3dd6-4ec9-a3b9-5ed03d0414bd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | United Urologics Closed System Catheter Kit |
Version Model Number | UU06K |
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 | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00818016020161 [Primary] |
GS1 | 10818016020168 [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 |