FDA UDI In Commercial Distribution 🇺🇸 United States

ENDOBON®

DI: 03599870091272 · Model: ROX20 · BIOMET 3I, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOBON®
Primary DI
03599870091272
Version / Model
ROX20
Company Name
BIOMET 3I, LLC
Labeler DUNS
186127825
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-10
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
de760c7e-c085-4a78-b6ec-b96560ee1167

Device Description

ENDOBON® XENOGRAFT GRANULES 2.0ML

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
LYC Bone grafting material, synthetic

GMDN Terms

Code Name
48097 Bone matrix implant, animal-derived, non-bioabsorbable

Identifiers

Type ID
Primary 03599870091272

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 2 Milliliter
Device Size Text, specify Particle Size 1 mm
Device Size Text, specify Particle Size 0.5 mm