FDA UDI In Commercial Distribution 🇺🇸 United States

BoneFoam

DI: 00810075280197 · Model: 925.SER · BONE FOAM, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BoneFoam
Primary DI
00810075280197
Version / Model
925.SER
Catalog Number
925.SER
Company Name
BONE FOAM, INC.
Labeler DUNS
079636174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-22
Public Version
2
Public Version Date
2023-04-11
Public Version Status
Update
Public Device Record Key
6cc33916-f3ab-4967-a316-607561e2c56d

Device Description

Semi-Extended Ramp

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CCX SUPPORT, PATIENT POSITION

GMDN Terms

Code Name
58878 Freestanding patient positioner, reusable

Identifiers

Type ID
Primary 00810075280197