Primary Device ID | 00886333001668 |
NIH Device Record Key | 93111d78-cb92-4214-9738-cd0aa997e4a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Introducer Sheath/Needle |
Version Model Number | 19 ga x 20 cm |
Catalog Number | ISN 1920 |
Company DUNS | 140727624 |
Company Name | ARGON MEDICAL DEVICES, INC. |
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 | 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 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333001668 [Primary] |
GS1 | 20886333001662 [Package] Package: Box [10 Units] In Commercial Distribution |
FGE | Catheter, Biliary, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2015-10-23 |
20886333224382 | Introducer Sheath/Needle 19ga x 15cm |
00886333001668 | Introducer Sheath/Needle |