FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10884389170793 · Model: MDTFUSION80 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10884389170793
Version / Model
MDTFUSION80
Catalog Number
MDTFUSION80
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-02
Public Version
1
Public Version Date
2022-12-12
Public Version Status
New
Public Device Record Key
5a74f1aa-caab-4d8a-a83a-0bd69cfe8f11

Device Description

MATTRESS,FUSION+, 36X80X6

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
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FNM MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE

GMDN Terms

Code Name
63237 Foam bed mattress

Identifiers

Type ID
Primary 10884389170793

Customer Contacts