FDA UDI In Commercial Distribution 🇺🇸 United States

Single Patient Use HoverMatt

DI: 00816299012187 · Model: RGMT39FL-REG · Hovertech International
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Single Patient Use HoverMatt
Primary DI
00816299012187
Version / Model
RGMT39FL-REG
Catalog Number
RGMT39FL-REG
Company Name
Hovertech International
Labeler DUNS
942139841
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-16
Public Version
1
Public Version Date
2023-01-24
Public Version Status
New
Public Device Record Key
4dfd3f44-1796-4463-a61a-1ac5e88d7878

Device Description

39" Single Patient Use Air Transfer Mattress: Regard(ROI)

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FRZ Device, Patient Transfer, Powered

GMDN Terms

Code Name
37160 Patient transfer system, powered

Identifiers

Type ID
Primary 00816299012187
Package 00816299012132

Customer Contacts

Device Sizes

Type Value Unit Text
Width 39 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 158 Degrees Fahrenheit