FDA UDI In Commercial Distribution 🇺🇸 United States

DuraFlow

DI: H787103003010 · Model: 10300301 · ANGIODYNAMICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DuraFlow
Primary DI
H787103003010
Version / Model
10300301
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
079105071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-15
Public Version
3
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
c2d706a1-dc8e-419f-a472-5c46f75f342d

Device Description

7F Double Access Hemodialysis Set

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
LFK CATHETER, FEMORAL
LFJ CATHETER, SUBCLAVIAN

GMDN Terms

Code Name
37278 Double-lumen haemodialysis catheter, implantable

Identifiers

Type ID
Package H787103003015
Primary H787103003010

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 7 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 27 Degrees Celsius