FDA UDI In Commercial Distribution 🇺🇸 United States

Coeur

DI: M297306010 · Model: C403-0601 · COEUR, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Coeur
Primary DI
M297306010
Version / Model
C403-0601
Catalog Number
C403-0601
Company Name
COEUR, INC.
Labeler DUNS
132515441
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-14
Public Version
3
Public Version Date
2019-02-04
Public Version Status
Update
Public Device Record Key
afb8967f-29e9-43d2-88d1-2562972655eb

Device Description

60 in. (1500mm) High Pressure Line with Rotating Adapter

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
44685 Radiographic procedure tubing

Identifiers

Type ID
Package M297306016
Package M297306015
Primary M297306010

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071196 000

Device Sizes

Type Value Unit Text
Length 1500 Millimeter
Length 60 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep product in clean, dry location. Avoid direct rays, heat and high humidity, and ultraviolet rays such as a germicidal light.