FDA UDI In Commercial Distribution 🇺🇸 United States

AVANTI

DI: 10705032010122 · Model: 504608D · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AVANTI
Primary DI
10705032010122
Version / Model
504608D
Catalog Number
504608D
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
a3e6d7a8-f401-4a61-a800-6bb8cfc43fff

Device Description

SI AVANTI+ 8F MID W/OBT

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 10705032010122
Package 20705032010129

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius