Primary Device ID | 20886333225907 |
NIH Device Record Key | 00f6197b-4291-49b6-86c4-fcdf5541031d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Co-Axial Cannula Bundle |
Version Model Number | MCXB1610BPU |
Catalog Number | MCXB1610BPU |
Company DUNS | 140727624 |
Company Name | ARGON MEDICAL DEVICES, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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 |
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 |
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 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00886333225903 [Primary] |
GS1 | 20886333225907 [Package] Contains: 00886333225903 Package: Box [5 Units] In Commercial Distribution |
MJG | Device, Percutaneous, Biopsy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-29 |
Device Publish Date | 2022-07-21 |
20886333225884 | Co-Axial Cannula Bundle 17ga x 11.8cm |
20886333225877 | Co-Axial Cannula Bundle 17ga x 6.8cm |
00886333225866 | Co-Axial Cannula Bundle 15ga x 11.8cm |
20886333225853 | Co-Axial Cannula Bundle 15ga x 6.8cm |
20886333225945 | Co-Axial Cannula Bundle 16ga x 16.8cm |
20886333225938 | Co-Axial Cannula Bundle 16ga x 11.8cm |
20886333225921 | Co-Axial Cannula Bundle 16ga x 6.8cm |
20886333225914 | Co-Axial Cannula Bundle 14ga x 11.8cm |
20886333225907 | Co-Axial Cannula Bundle 14ga x 6.8cm |
20886333225891 | Co-Axial Cannula Bundle 17ga x 16.8cm |
20886333226393 | Co-Axial Cannula Bundle 19ga x 16.0cm |
20886333226386 | Co-Axial Cannula Bundle 19ga x 12.0cm |
20886333226379 | Co-Axial Cannula Bundle 19ga x 6.0cm |
20886333226362 | Co-Axial Cannula Bundle 17ga x 20.5cm |
20886333226355 | Co-Axial Cannula Bundle 17ga x 15.5cm |
20886333226348 | Co-Axial Cannula Bundle 17ga x 11.5cm |
20886333226331 | Co-Axial Cannula Bundle 17ga x 5.5cm |