FDA UDI In Commercial Distribution 🇺🇸 United States

Omnilink Elite

DI: 08717648178504 · Model: 1012631-29 · ABBOTT VASCULAR INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Omnilink Elite
Primary DI
08717648178504
Version / Model
1012631-29
Catalog Number
1012631-29
Company Name
ABBOTT VASCULAR INC.
Labeler DUNS
964569052
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-21
Public Version
4
Public Version Date
2023-08-01
Public Version Status
Update
Public Device Record Key
d88eaf68-63c9-4157-b036-a2382c4e11c3

Device Description

Omnilink Elite Vascular Balloon-Expandable Stent System 8.0 mm x 29 mm x 135 cm Over-The-Wire

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
MR Conditional
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
NIO STENT, ILIAC

GMDN Terms

Code Name
47932 Peripheral artery stent, bare-metal

Identifiers

Type ID
Primary 08717648178504

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep dry, keep away from sunlight, temperature limitation 15 to 30 degrees C (59 F to 86 degrees F)