Primary Device ID | 04035324054817 |
NIH Device Record Key | eecc5932-d613-49d5-8301-ddd653b5a1c4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRACOE modular |
Version Model Number | REF 640-CT |
Catalog Number | REF 640-CT |
Company DUNS | 319414785 |
Company Name | Tracoe medical GmbH |
Device Count | 50 |
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 | 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 |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com | |
Phone | +49613691690 |
info@tracoe.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from rain. Keep away from sunlight. Do not use if package is damaged and consult IFU. Do not resterilize. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04035324054817 [Primary] |
GS1 | 05701780328388 [Unit of Use] |
BYD | CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-11-29 |
Device Publish Date | 2015-10-18 |
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