FDA UDI In Commercial Distribution 🇺🇸 United States

C3 WAVE SYSTEM

DI: H787MRC3S900 · Model: MRC3S90 · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
C3 WAVE SYSTEM
Primary DI
H787MRC3S900
Version / Model
MRC3S90
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
079105071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-08
Public Version
1
Public Version Date
2022-04-18
Public Version Status
New
Public Device Record Key
34bd7687-198e-4a8f-9024-18c8d3803273

Device Description

C3 WAVE HUB ACCESSORY

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LJS Catheter, intravascular, therapeutic, long-term greater than 30 days

GMDN Terms

Code Name
61564 Central venous catheter navigation system, electrocardiographic

Identifiers

Type ID
Secondary 15051684027236
Primary H787MRC3S900

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180567 000