FDA UDI Not in Commercial Distribution 🇺🇸 United States

Vista®

DI: 04046964188138 · Model: US9922F · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Vista®
Primary DI
04046964188138
Version / Model
US9922F
Catalog Number
US9922F
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2020-10-23
Public Version Status
Update
Public Device Record Key
b7bf32cb-d157-4d0d-a4f1-2f6a5e9fa131
Distribution End Date
2020-10-21

Device Description

15 drops/mL, free flow protection, Priming volume 20.7mL, length 102in.

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
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
FPA Set, administration, intravascular

GMDN Terms

Code Name
35833 Electric infusion pump administration set, single-use

Identifiers

Type ID
Primary 04046964188138
Unit of Use 04046964188121

Customer Contacts