Primary Device ID | 10840619033559 |
NIH Device Record Key | a7c330c8-aa23-4993-af49-5d18d156fb27 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Transpac |
Version Model Number | 42587-05 |
Company DUNS | 118380146 |
Company Name | ICU MEDICAL, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840619033552 [Primary] |
GS1 | 10840619033559 [Package] Contains: 00840619033552 Package: [20 Units] In Commercial Distribution |
KRA | Catheter, continuous flush |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2017-12-18 |
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