FDA UDI In Commercial Distribution 🇺🇸 United States

MedicaPure

DI: 00817411021971 · Model: AC+225 · NIPRO RENAL SOLUTIONS USA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MedicaPure
Primary DI
00817411021971
Version / Model
AC+225
Company Name
NIPRO RENAL SOLUTIONS USA CORPORATION
Labeler DUNS
117439434
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-25
Public Version
1
Public Version Date
2021-07-05
Public Version Status
New
Public Device Record Key
d812fb08-44ea-45e9-bdb4-74a9d9c08542

Device Description

Liquid Acid Concentrate

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
No
Sterilization Prior Use
No

Product Codes

Code Name
KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

GMDN Terms

Code Name
35849 Haemodialysis concentrate

Identifiers

Type ID
Package 10817411021978
Primary 00817411021971
Previous 00817411021018

Premarket Submissions

Submission Number Supplement Number
K901471 000