FDA UDI In Commercial Distribution 🇺🇸 United States

RESORBA Synthetic Bone

DI: 03700501813440 · Model: SB0701M+G50 · BIOMATLANTE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RESORBA Synthetic Bone
Primary DI
03700501813440
Version / Model
SB0701M+G50
Catalog Number
SB0701M+G50
Company Name
BIOMATLANTE
Labeler DUNS
493710719
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-17
Public Version
1
Public Version Date
2024-05-27
Public Version Status
New
Public Device Record Key
1407e67d-b146-42af-bf57-c5bd0b9a3c47

Device Description

Synthetic Bone Substitute HA/BTCP ratio 20/80 Resorbable Bone Graft Granules 0.5-1 mm (0.5 cm3) Syringe (x1)

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
Yes
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
LYC Bone Grafting Material, Synthetic

GMDN Terms

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

Identifiers

Type ID
Primary 03700501813440

Premarket Submissions

Submission Number Supplement Number
K093122 000