FDA UDI In Commercial Distribution 🇺🇸 United States

PulseSpray

DI: H787125004080 · Model: 12500408 · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
PulseSpray
Primary DI
H787125004080
Version / Model
12500408
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
079105071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
7
Public Version Date
2023-10-23
Public Version Status
Update
Public Device Record Key
67180c3a-3d5d-4ff1-860a-e5cd0e760b57

Device Description

PulseSpray Infusion System

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
KRA Catheter, continuous flush

GMDN Terms

Code Name
32151 Peripheral vascular intervention infusion catheter

Identifiers

Type ID
Package H787125004085
Primary H787125004080
Secondary 15051684013147

Customer Contacts

Device Sizes

Type Value Unit Text
Length 90 Centimeter
Catheter Gauge 5 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 27 Degrees Celsius