FDA UDI In Commercial Distribution 🇺🇸 United States

HoverMatt PROS

DI: 00816299012569 · Model: PROS-SS · Hovertech International
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HoverMatt PROS
Primary DI
00816299012569
Version / Model
PROS-SS
Company Name
Hovertech International
Labeler DUNS
942139841
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-10
Public Version
1
Public Version Date
2025-09-18
Public Version Status
New
Public Device Record Key
319bf6ea-aeb4-4697-9371-feb8f3a2999b

Device Description

HoverMatt PROS Slide Sheet

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FMR Device, Transfer, Patient, Manual

GMDN Terms

Code Name
37165 Patient transfer/turning sheet, single-use

Identifiers

Type ID
Primary 00816299012569