FDA UDI Not in Commercial Distribution 🇺🇸 United States

Universal SteriBump®

DI: 00696588005607 · Model: 508.1 · Innovative Medical Products, Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Universal SteriBump®
Primary DI
00696588005607
Version / Model
508.1
Catalog Number
508.1
Company Name
Innovative Medical Products, Inc
Labeler DUNS
147363154
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-05
Public Version
2
Public Version Date
2020-05-13
Public Version Status
Update
Public Device Record Key
8694620c-3c8d-4317-a766-b84e091ec409
Distribution End Date
2020-05-12

Device Description

Universal SteriBump® Sample

Device Characteristics

Single Use
Yes
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
Yes
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
Yes
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 00696588005607