FDA UDI Not in Commercial Distribution 🇺🇸 United States

SAVVY

DI: 20705032006207 · Model: 435300L · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SAVVY
Primary DI
20705032006207
Version / Model
435300L
Catalog Number
435300L
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
6
Public Version Date
2023-10-12
Public Version Status
Update
Public Device Record Key
1253291e-3f98-4c0e-b68a-a91b7c7d1099
Distribution End Date
2019-09-30

Device Description

PTA SAVVY SMALL VESSEL 3X10

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

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 20705032006207

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dark, dry place
Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damanged