Primary Device ID | 20886333004953 |
NIH Device Record Key | 53e3a727-09d3-41c0-87ef-178b3dfbf848 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Screw Dilator |
Version Model Number | 631438025 |
Catalog Number | 631438025 |
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 | 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 |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com | |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333004959 [Primary] |
GS1 | 20886333004953 [Package] Contains: 00886333004959 Package: Box [10 Units] In Commercial Distribution |
GCC | Dilator, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-12 |
20886333004960 | Screw Dilator 16F x 25cm |
20886333004953 | Screw Dilator 14F x 25cm |
20886333004946 | Screw Dilator 12F x 25cm |
20886333004939 | Screw Dilator 10F x 25cm |
20886333004922 | Screw Dilator 9F x 25cm |
20886333004915 | Screw Dilator 8F x 25cm |
20886333004908 | Screw Dilator 7Fr x 25cm |