FDA UDI In Commercial Distribution 🇺🇸 United States

INFINITI™ AMBI

DI: 10705032100069 · Model: 555600J402 · Cordis US Corp.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
INFINITI™ AMBI
Primary DI
10705032100069
Version / Model
555600J402
Catalog Number
555600J402
Company Name
Cordis US Corp.
Labeler DUNS
118274128
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-16
Public Version
1
Public Version Date
2024-02-26
Public Version Status
New
Public Device Record Key
bc0a9147-89c4-4a95-8667-5afba8f79c78

Device Description

6F INFINITI AMBI 100CM JK 4.0

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
DQO Catheter, intravascular, diagnostic

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 20705032100066
Primary 10705032100069