FDA UDI In Commercial Distribution 🇺🇸 United States

Bibag

DI: 00840861101320 · Model: 08-4080-BB · Fresenius Medical Care Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Bibag
Primary DI
00840861101320
Version / Model
08-4080-BB
Catalog Number
08-4080-BB
Company Name
Fresenius Medical Care Holdings, Inc.
Labeler DUNS
958291411
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-02
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4882615d-989a-4d7b-b033-291ebc39c31d

Device Description

Bibag Dry Sodium Bicarbonate

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 10840861101327
Primary 00840861101320

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not refrigerate. Keep bag tightly sealed until it is connected to the hemodialysis machine