FDA UDI In Commercial Distribution 🇺🇸 United States

PROS Wedge

DI: 00816299012729 · Model: PROS-WEDGE · Hovertech International
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
PROS Wedge
Primary DI
00816299012729
Version / Model
PROS-WEDGE
Catalog Number
PROS-WEDGE
Company Name
Hovertech International
Labeler DUNS
942139841
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-16
Public Version
1
Public Version Date
2024-04-24
Public Version Status
New
Public Device Record Key
c19adf01-c693-4d56-9942-7f281ccc1061

Device Description

PROS Wedge

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
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
FMP Protector, Skin Pressure

GMDN Terms

Code Name
62292 Freestanding patient positioner, single-use

Identifiers

Type ID
Primary 00816299012729
Package 00816299012743
Package 00816299012767

Customer Contacts