Primary Device ID | 00850082007127 |
NIH Device Record Key | 17763978-1902-4490-a852-851794b2dc8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aspiration Tubing |
Version Model Number | 51412 |
Company DUNS | 797391778 |
Company Name | ARMM INC. |
Device Count | 10 |
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 |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com | |
Phone | 7148488190 |
info@armminc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850082007127 [Unit of Use] |
GS1 | 10850082007124 [Primary] |
KDH | Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-16 |
Device Publish Date | 2023-06-08 |
00850082007127 | Aspiration Tubing - 12' |
00850082007110 | Aspiration Tubing - 10' |
00850082007103 | Aspiration Tubing - 8' |