Primary Device ID | 10813153028039 |
NIH Device Record Key | 38c01a99-243d-4525-aee9-ab41c5a12938 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LABEL PRODUCT -CODAN |
Version Model Number | BC111 |
Company DUNS | 058027475 |
Company Name | Codan US 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 | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813153028032 [Package] Package: MULTIVAC PACKAGING [1 Units] In Commercial Distribution |
GS1 | 10813153028039 [Primary] |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-09 |
Device Publish Date | 2025-05-30 |
00813153022672 | Extension Set with Needle Valve & Needlefree T-connector |
00813153022344 | Extension Set with Spin-Lock |
10813153028039 | One Way Stopcock with Rotating Male Luer lock |
00813153022955 | Bifurcated Blood Set with Spin-lock |
00813153021613 | IV Extension Set with Stopcock, Injection Sites, & T-connector |