FDA UDI Not in Commercial Distribution 🇺🇸 United States

AVAflex

DI: 10885403241178 · Model: AFB1115 · CAREFUSION 2200, INC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AVAflex
Primary DI
10885403241178
Version / Model
AFB1115
Catalog Number
AFB1115
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-01
Public Version
3
Public Version Date
2023-10-03
Public Version Status
Update
Public Device Record Key
aac30b44-e6dd-45de-8d74-80d63c8b22cc
Distribution End Date
2018-04-12

Device Description

AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX15MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
HRX Arthroscope
NDN Cement, Bone, Vertebroplasty

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Package 50885403241176
Primary 10885403241178

Device Sizes

Type Value Unit Text
Length 15 Millimeter
Needle Gauge 11 Gauge

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius