FDA UDI In Commercial Distribution 🇺🇸 United States

PRO OSTEON 500R

DI: 00888480584902 · Model: 5RBW108 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRO OSTEON 500R
Primary DI
00888480584902
Version / Model
5RBW108
Catalog Number
5RBW108
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
b6a8c220-b029-4469-b053-a2bbf9d79536

Device Description

Resorbable Bone Graft Substitute Block, W-Block

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00888480584902

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 12 mm X 25 mm X 60 mm Block (10.8 cc)