FDA UDI In Commercial Distribution 🇺🇸 United States

PUREFLOW SL

DI: M535NX200010 · Model: NX2000-1 · NXSTAGE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PUREFLOW SL
Primary DI
M535NX200010
Version / Model
NX2000-1
Company Name
NXSTAGE MEDICAL, INC.
Labeler DUNS
088013219
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2c71260e-90f9-4e38-8607-717293cff10d

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FKR Subsystem, Proportioning

GMDN Terms

Code Name
34994 Haemodialysis system dialysate delivery unit

Identifiers

Type ID
Primary M535NX200010

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius