FDA UDI In Commercial Distribution 🇺🇸 United States

Fusion DF

DI: 00817365021676 · Model: FUSXL4280DF · MOXI ENTERPRISES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fusion DF
Primary DI
00817365021676
Version / Model
FUSXL4280DF
Company Name
MOXI ENTERPRISES, LLC
Labeler DUNS
958807575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-25
Public Version
2
Public Version Date
2019-06-28
Public Version Status
Update
Public Device Record Key
a05a801e-1c19-41e7-8761-87f3eed21bce

Device Description

FUSION 42x80x8 Mattress with Dry Floatation Insert

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKY Mattress, Flotation Therapy, Non-Powered

GMDN Terms

Code Name
47520 Orthopaedic bed mattress

Identifiers

Type ID
Primary 00817365021676