Primary Device ID | 00817365022215 |
NIH Device Record Key | f80f9ff0-af6d-4969-a3d0-da64a2de62b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fusion 2KXL |
Version Model Number | FUS4880COV |
Catalog Number | FUS4880COV |
Company DUNS | 958807575 |
Company Name | MOXI ENTERPRISES, LLC |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com | |
Phone | 314-771-5222 |
info@moxiusa.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817365022215 [Primary] |
FMW | Cover, Mattress (Medical Purposes) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-14 |
Device Publish Date | 2022-11-04 |
00817365022215 | Fusion 2KXL Outer Cover 48x80x8 |
00817365022208 | Fusion 2KXL Outer Cover 42x84x8 |
00817365022192 | Fusion 2KXL Outer Cover 42x80x8 |