FDA UDI In Commercial Distribution 🇺🇸 United States

iVAS

DI: 07613327358308 · Model: 808010800 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
iVAS
Primary DI
07613327358308
Version / Model
808010800
Catalog Number
0808-010-800
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-11
Public Version
3
Public Version Date
2020-07-09
Public Version Status
Update
Public Device Record Key
5cd91e91-c293-4dac-a157-08eb3d05153b

Device Description

10 gauge 10mm iVAS Elite Fracture Kit

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
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
Primary 07613327358308
Package 37613327358309

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 10.0 Gauge
Device Size Text, specify Balloon Length: 10.0 Millimeter

Storage Conditions

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