Primary Device ID | 00894912002166 |
NIH Device Record Key | 514dcc54-01be-4d47-b7a2-39f9ba70f8aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CT |
Version Model Number | CT-7 |
Catalog Number | CT-7 |
Company DUNS | 069261402 |
Company Name | KOVEN TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com | |
Phone | 314-542-2101 |
info@koven.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00894912002166 [Primary] |
BZN | Cart, Emergency, Cardiopulmonary (Excluding Equipment) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-01-28 |
Device Publish Date | 2021-01-20 |
00894912002142 | Doppler rollcart |
00894912002081 | Doppler roll cart |
00894912002036 | Doppler roll cart |
00894912002012 | Doppler roll cart |
00894912002005 | Doppler roll cart |
00894912002166 | Doppler roll cart for BiDop 7 |