FDA UDI In Commercial Distribution 🇺🇸 United States

DIASOL

DI: B467BP4512 · Model: BP10000X12 · DIASOL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
DIASOL
Primary DI
B467BP4512
Version / Model
BP10000X12
Catalog Number
BP6/7
Company Name
DIASOL, INC.
Labeler DUNS
068434658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-28
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
3a7d8b1c-b6d7-4477-84d2-223b7fa5fbe8

Device Description

Diasol Sodium Bicarbonate Powder

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
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
Primary B467BP4512
Package B467BP5612T1
Package B467BP4512T3

Customer Contacts

Phone
818-838-7077

Premarket Submissions

Submission Number Supplement Number
K020230 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Bicarbonate base concentrate should be used within 24 hours of being mixed. Keep in a closed container to minimize CO2 loss and resulting precipitation. Do not use bag if seal is broken.