FDA UDI In Commercial Distribution 🇺🇸 United States

Hemoflow™

DI: 00840861100026 · Model: 0520161A · Fresenius Medical Care Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Hemoflow™
Primary DI
00840861100026
Version / Model
0520161A
Company Name
Fresenius Medical Care Holdings, Inc.
Labeler DUNS
958291411
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
6
Public Version Date
2024-02-26
Public Version Status
Update
Public Device Record Key
e0f5b415-e033-4b3a-a2af-aa9975914960

Device Description

F4 Hemoflow Dialyzer / Low Flux / Polysulfone / 0.7 m2 / ETO / Low Volume / Single Use / 45 mL

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
FJI DIALYZER, CAPILLARY, HOLLOW FIBER

GMDN Terms

Code Name
47072 Hollow-fibre haemodialysis dialyser, single-use

Identifiers

Type ID
Package 10840861100023
Primary 00840861100026

Customer Contacts

Device Sizes

Type Value Unit Text
Area/Surface Area 0.7 Square meter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 27 Degrees Celsius