AccessGUDID - DEVICE: AVAmax (10885403001932)

GUDID

Device Identifier (DI) Information

Brand Name: AVAmax
Version or Model: VBT0820
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: VBT0820
Company Name: CAREFUSION 2200, INC

Primary DI Number: 10885403001932
Issuing Agency: GS1
Commercial Distribution End Date: April 12, 2018
Device Count: 1
Labeler D-U-N-S® Number*: 832696038 *Terms of Use

Device Description: AVAMAX™ VERTEBRAL BALLOON TRAY 8GX20MM

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
47129	Balloon kyphoplasty kit	A collection of sterile surgical instruments and devices used for the reduction of a vertebral compression fractures (VCFs) caused by trauma, cancer, or osteoporosis during a minimally invasive procedure commonly known as balloon kyphoplasty. It typically consists of a bone access needle, an osteo introducer, an inflation syringe, and the inflatable bone tamp. This procedure involves the insertion of the balloon tamp into a patient's back to reduce a vertebral body fracture by compression of cancellous bone and/or movement of the endplates as the balloon is inflated, and filling the void created with orthopaedic cement/filler to stabilize the vertebra. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HRX	Arthroscope
NDN	Cement, Bone, Vertebroplasty

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Ethylene Oxide

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 0 and 50 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Length: 20 Millimeter
Needle Gauge: 8 Gauge

Device Record Status

Public Device Record Key: f045e4fe-2202-4f64-b209-01267300fe4a
Public Version Date: October 04, 2023
Public Version Number: 3
DI Record Publish Date: October 24, 2015