FDA UDI Not in Commercial Distribution 🇺🇸 United States

iVAS

DI: 07613252505983 · Model: 0705310000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
iVAS
Primary DI
07613252505983
Version / Model
0705310000
Catalog Number
0705-310-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
9
Public Version Date
2021-11-18
Public Version Status
Update
Public Device Record Key
994fa122-8225-48bf-9e38-35f3dfcd2ece
Distribution End Date
2021-07-08

Device Description

Inflatable Vertebral Augmentation System

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
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
NDN CEMENT, BONE, VERTEBROPLASTY

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Package 37613252505984
Primary 07613252505983

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 11.0 Gauge
Length 10.0 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
12 – 25 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 60 Percent (%) Relative Humidity