Primary Device ID | 14580303269036 |
NIH Device Record Key | 1d7416d1-65d8-41e7-97bd-bcf96675e3fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kitazato IUI Catheter without Stainless Steel Center Core Type1-v2 |
Version Model Number | 101073 Type2-v2 |
Catalog Number | 101073 |
Company DUNS | 711091157 |
Company Name | KITAZATO CORPORATION |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04580303269039 [Primary] |
GS1 | 14580303269036 [Package] Contains: 04580303269039 Package: [10 Units] In Commercial Distribution |
MQF | CATHETER, ASSISTED REPRODUCTION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2016-11-09 |
14580745043775 - ET Catheter | 2024-09-17 ET Catheter |
14580745043898 - ET Catheter | 2024-09-17 ET Catheter |
14580745044260 - ET Catheter | 2024-09-17 ET Catheter |
14580745044284 - ET Catheter | 2024-09-17 ET Catheter |
14582231462961 - ES - Equilibration Solution | 2024-09-16 Individual vial 1.5 ml |
14580745043706 - OPU Needle | 2024-05-24 1 Packs |
14580745043720 - OPU Needle | 2024-05-24 1 Packs |
14580745043737 - OPU Needle | 2024-05-24 1 Packs |