FDA UDI In Commercial Distribution 🇺🇸 United States

Armada

DI: 08717648155246 · Model: B2050-250 · ABBOTT VASCULAR INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Armada
Primary DI
08717648155246
Version / Model
B2050-250
Catalog Number
B2050-250
Company Name
ABBOTT VASCULAR INC.
Labeler DUNS
964569052
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-15
Public Version
7
Public Version Date
2020-03-23
Public Version Status
Update
Public Device Record Key
79d77964-cdd1-4ff4-a00a-5e0eb17c19f0

Device Description

Armada 35 LL PTA Catheter 5 mm x 250 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
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
LIT Catheter, angioplasty, peripheral, transluminal
DQY CATHETER, PERCUTANEOUS

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 08717648155246

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dark, dry and cool place. Do not expose to organic solvents, ionizing radiation or ultraviolet light.
Type
Storage Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit