FDA UDI In Commercial Distribution 🇺🇸 United States

Coeur/Nemoto

DI: M902124200 · Model: C453-2420 · COEUR, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Coeur/Nemoto
Primary DI
M902124200
Version / Model
C453-2420
Catalog Number
C453-2420
Company Name
COEUR, INC.
Labeler DUNS
132515441
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-28
Public Version
1
Public Version Date
2018-09-28
Public Version Status
New
Public Device Record Key
372058fa-bda4-4e17-84ef-bf385653578e

Device Description

1200 PSI High Pressure Y-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 M902124206
Package M902124205
Primary M902124200

Premarket Submissions

Submission Number Supplement Number
K071196 000

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.