FDA UDI In Commercial Distribution 🇺🇸 United States

MICROFUSE

DI: 00849044044218 · Model: 838.137S · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MICROFUSE
Primary DI
00849044044218
Version / Model
838.137S
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-08
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
dc995b76-7b5c-4ebf-9341-e981e45e57eb

Device Description

MicroFuse LT Slotted Block, w/BaSO4/CaSO4, 14mm x 12mm x 10mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
16966 Synthetic bone graft

Identifiers

Type ID
Primary 00849044044218

Customer Contacts

Device Sizes

Type Value Unit Text
Length 12 Millimeter
Height 10 Millimeter
Width 14 Millimeter