FDA UDI In Commercial Distribution 🇺🇸 United States

C3 WAVE SYSTEM

DI: H787MRC3S950 · Model: MRC3S95 · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
C3 WAVE SYSTEM
Primary DI
H787MRC3S950
Version / Model
MRC3S95
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
2
Public Version Date
2024-03-25
Public Version Status
Update
Public Device Record Key
fcbf9c04-5848-4bda-9bc2-2a463e8edf8c

Device Description

C3 WAVE IPAD CASE 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
No
Has Lot/Batch Number
Yes
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 15051684027373
Primary H787MRC3S950

Customer Contacts