FDA UDI Not in Commercial Distribution 🇺🇸 United States

MAR0Fuse

DI: M896MAR0FUSE1CC1 · Model: MAR0Fuse1cc · ARTERIOCYTE MEDICAL SYSTEMS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAR0Fuse
Primary DI
M896MAR0FUSE1CC1
Version / Model
MAR0Fuse1cc
Company Name
ARTERIOCYTE MEDICAL SYSTEMS, INC.
Labeler DUNS
809012870
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-13
Public Version
3
Public Version Date
2019-11-13
Public Version Status
Update
Public Device Record Key
7a8f9112-5348-4510-8ded-b3096e427f99
Distribution End Date
2019-11-12

Device Description

MAR0Fuse Demineralized Bone Matrix Gel

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Primary M896MAR0FUSE1CC1

Customer Contacts

Phone
8666602674

Device Sizes

Type Value Unit Text
Total Volume 1 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius