FDA UDI In Commercial Distribution 🇺🇸 United States

Diacap®

DI: 04046955659661 · Model: 720DH19G · B.Braun Avitum AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Diacap®
Primary DI
04046955659661
Version / Model
720DH19G
Catalog Number
720DH19G
Company Name
B.Braun Avitum AG
Labeler DUNS
343689704
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2022-09-16
Public Version
1
Public Version Date
2022-09-26
Public Version Status
New
Public Device Record Key
46fa514d-d372-4ff8-8fc1-dbb06e61ef1e

Device Description

Diacap Pro 19H G

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

GMDN Terms

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

Identifiers

Type ID
Unit of Use 04046955659654
Primary 04046955659661

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Max TMP (mmHg) : 600.000 MHG
Device Size Text, specify Max TMP (kPa) : 80.000 KPA
Device Size Text, specify Volume Blood Compartment : 120.000 ML
Device Size Text, specify Surface (m²) : 1.900 M2

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 30 Degrees Celsius