Primary Device ID | 14580303269319 |
NIH Device Record Key | 2f2201bc-1580-421a-acf5-51bcfa36f315 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kitazato OPU Reduced Needle, Type3-v6 |
Version Model Number | 341002 Type 3-v6 |
Catalog Number | 341002 |
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 | 04580303269312 [Primary] |
GS1 | 14580303269319 [Package] Contains: 04580303269312 Package: [10 Units] In Commercial Distribution |
MQE | NEEDLE, ASSISTED REPRODUCTION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-08 |
Device Publish Date | 2018-05-30 |
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 |