FDA UDI In Commercial Distribution 🇺🇸 United States

AVANTI

DI: 10705032010290 · Model: 504617Z · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AVANTI
Primary DI
10705032010290
Version / Model
504617Z
Catalog Number
504617Z
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
7
Public Version Date
2022-09-14
Public Version Status
Update
Public Device Record Key
dbc09929-b994-4053-8263-0d8632c7f4b9

Device Description

SI AVANTI+ TRANSRAD KIT 11CM

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
Yes
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
DRE DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

GMDN Terms

Code Name
36079 Haemostasis valve

Identifiers

Type ID
Primary 10705032010290
Package 20705032010297

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius