FDA UDI In Commercial Distribution 🇺🇸 United States

AVANTI

DI: 10705032010399 · Model: 504657A · Cordis US Corp.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
AVANTI
Primary DI
10705032010399
Version / Model
504657A
Catalog Number
504657A
Company Name
Cordis US Corp.
Labeler DUNS
118274128
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
9
Public Version Date
2025-12-15
Public Version Status
Update
Public Device Record Key
9c43cf59-8497-48bf-9c4c-fe6deb4fb28e

Device Description

CSI AVANTI+ CARDIOLOGY MS .038

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 10705032010399
Package 20705032010396

Premarket Submissions

Submission Number Supplement Number
K970392 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius