FDA UDI In Commercial Distribution 🇺🇸 United States

PRISMAFLEX SET M150

DI: 07332414201364 · Model: 109990MDR · Vantive Health GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRISMAFLEX SET M150
Primary DI
07332414201364
Version / Model
109990MDR
Catalog Number
109990MDR
Company Name
Vantive Health GmbH
Labeler DUNS
480723888
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-27
Public Version
1
Public Version Date
2026-04-06
Public Version Status
New
Public Device Record Key
0c61b784-e219-4eff-935b-adc8bdd3adf8

Device Description

The Prismaflex M150 set is indicated for use only with the PrismaFlex control unit or with the PrisMax control unit (in countries where PrisMax is cleared or registered) in providing continuous fluid management and renal replacement therapies. The system is intended for patients who have acute renal failure, fluid overload, or both.

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
Yes
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
KDI Dialyzer, high permeability with or without sealed dialysate system

GMDN Terms

Code Name
44601 Haemofilter

Identifiers

Type ID
Package 57332414201369
Primary 07332414201364

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080519 000

Device Sizes

Type Value Unit Text
Length 27 Centimeter
Width 22 Centimeter
Height 9 Centimeter
Weight 874 Gram

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store the Prismaflex set in a dry place, between 0° C (32° F) and 30° C (86° F).