FDA UDI In Commercial Distribution 🇺🇸 United States

FIBERGRAFT BG Morsels

DI: 00856879006052 · Model: 4600-0040 · Prosidyan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FIBERGRAFT BG Morsels
Primary DI
00856879006052
Version / Model
4600-0040
Catalog Number
4600-0040
Company Name
Prosidyan, Inc.
Labeler DUNS
963425488
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-28
Public Version
6
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
697d3d46-15ee-4cde-8efc-e32a7815cf7c

Device Description

4cc vial of Fibergraft BG Morsels bioactive bone graft substitute

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
Yes
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 00856879006052

Customer Contacts

Phone
908-517-3666

Premarket Submissions

Submission Number Supplement Number
K151154 000