FDA UDI Not in Commercial Distribution 🇺🇸 United States

Diacap®

DI: 04046964319921 · Model: 7204001 · B.Braun Avitum AG
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Diacap®
Primary DI
04046964319921
Version / Model
7204001
Catalog Number
7204001
Company Name
B.Braun Avitum AG
Labeler DUNS
343689704
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2015-08-09
Public Version
5
Public Version Date
2021-08-20
Public Version Status
Update
Public Device Record Key
5a1b4197-0686-4cb2-b4f5-69089e91e8c5
Distribution End Date
2019-02-09

Device Description

Diacap? Polysulfone® LOPS 12

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FJI DIALYZER, CAPILLARY, HOLLOW FIBER
KDI Dialyzer, high permeability with or without sealed dialysate system

GMDN Terms

Code Name
47072 Hollow-fibre haemodialysis dialyser, single-use

Identifiers

Type ID
Primary 04046964319921
Unit of Use 04039239089711

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 30 Degrees Celsius