FDA UDI In Commercial Distribution 🇺🇸 United States

Diapact®

DI: 04039239047346 · Model: 7210518 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
Diapact®
Primary DI
04039239047346
Version / Model
7210518
Catalog Number
7210518
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2015-08-09
Public Version
5
Public Version Date
2020-04-09
Public Version Status
Update
Public Device Record Key
79187d9e-95d7-4249-8840-fb3031fdd5fa

Device Description

Plasma Exchange (PEX) Tubing Set

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
FJK SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE

GMDN Terms

Code Name
47572 Apheresis system tubing set

Identifiers

Type ID
Primary 04039239047346
Unit of Use 04039239047339

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 30 Degrees Celsius