FDA UDI In Commercial Distribution 🇺🇸 United States

AUGMENT® Injectable

DI: 10859477002140 · Model: K30003010 · Biomimetic Therapeutics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AUGMENT® Injectable
Primary DI
10859477002140
Version / Model
K30003010
Catalog Number
K30003010
Company Name
Biomimetic Therapeutics, LLC
Labeler DUNS
078774659
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-12
Public Version
4
Public Version Date
2023-07-20
Public Version Status
Update
Public Device Record Key
75fb106e-9209-4d4f-b7d8-d7116b849e1a

Device Description

Injectable Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NOX Filler, Bone Void, Synthetic Peptide

GMDN Terms

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

Identifiers

Type ID
Primary 10859477002140

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 3.0 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Do not Freeze