FDA UDI In Commercial Distribution 🇺🇸 United States

Polyflux

DI: 07332414048181 · Model: 21L · Gambro Dialysatoren GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Polyflux
Primary DI
07332414048181
Version / Model
21L
Catalog Number
104176
Company Name
Gambro Dialysatoren GmbH
Labeler DUNS
316150549
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-12
Public Version
7
Public Version Date
2023-08-10
Public Version Status
Update
Public Device Record Key
bb5f947c-b7ca-46e1-a83f-3d6cff1d6db8

Device Description

The Polyflux 21L is intended for use in haemodialysis for the treatment of chronic or acute renal failure

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
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 37332414048182
Primary 07332414048181

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K043342 000

Device Sizes

Type Value Unit Text
Area/Surface Area 2.1 Square meter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 30 Degrees Celsius