FDA UDI In Commercial Distribution 🇺🇸 United States

Absolute Pro

DI: 08717648176289 · Model: 1012538-40 · ABBOTT VASCULAR INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Absolute Pro
Primary DI
08717648176289
Version / Model
1012538-40
Catalog Number
1012538-40
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
de31aabc-2533-4e64-bb78-a3512ceca227

Device Description

Absolute Pro Vascular Self-Expanding Stent System 10.0 mm x 40 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 08717648176289

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature only.
Type
Handling Environment Temperature
Temperature Range
-20 – 54 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-20 – 54 Degrees Celsius