FDA UDI Not in Commercial Distribution 🇺🇸 United States

Optiflux® Ultra

DI: 00840861100217 · Model: 0500421E · Fresenius Medical Care Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Optiflux® Ultra
Primary DI
00840861100217
Version / Model
0500421E
Company Name
Fresenius Medical Care Holdings, Inc.
Labeler DUNS
958291411
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2022-05-05
Public Version Status
Update
Public Device Record Key
73a79ba9-9176-4bfa-989c-8de1f2ceaa1c
Distribution End Date
2015-09-24

Device Description

F210 Optiflux Ultra Dialyzer / High Flux / Polysulfone / 2.2 m2 / Ebeam / Single Use / 124 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
KDI Dialyzer, high permeability with or without sealed dialysate system

GMDN Terms

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

Identifiers

Type ID
Package 10840861100214
Primary 00840861100217

Customer Contacts

Device Sizes

Type Value Unit Text
Area/Surface Area 2.2 Square meter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius