Primary Device ID | 14580303269593 |
NIH Device Record Key | 1c5181f2-385c-4b3a-bcc9-dd0060ec7f42 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kitazato ET Catheter Type2-v6 EC-PRO Supported |
Version Model Number | 205123 Type2-v6 EC-PRO Supported |
Catalog Number | 205123 |
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 | 04580303269596 [Primary] |
GS1 | 14580303269593 [Package] Contains: 04580303269596 Package: [10 Units] In Commercial Distribution |
MQF | CATHETER, ASSISTED REPRODUCTION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-07 |
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