Primary Device ID | 04046964578588 |
NIH Device Record Key | e0609b7f-bf7c-4cd1-939b-44411af03f78 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tri-Connector |
Version Model Number | 470152 |
Catalog Number | 470152 |
Company DUNS | 002397347 |
Company Name | B. BRAUN MEDICAL INC. |
Device Count | 50 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04046964578571 [Unit of Use] |
GS1 | 04046964578588 [Primary] |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-19 |
Device Publish Date | 2016-09-23 |
04046964578588 | TRI-CONNECTOR W/ FEMALE LL CONNECTOR |
04046964184611 | AET300 TRICONN / REFLUX VLVES |