FDA UDI Not in Commercial Distribution 🇺🇸 United States

Alaris, SmartSite

DI: 10885403421983 · Model: 72023KE · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Alaris, SmartSite
Primary DI
10885403421983
Version / Model
72023KE
Catalog Number
72023KE
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2024-07-26
Public Version Status
Update
Public Device Record Key
db388976-69ac-4012-a95f-9d1e29294072
Distribution End Date
2021-08-10

Device Description

SE PRI 20D 2SS VLVS

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
FPA Set, administration, intravascular

GMDN Terms

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

Identifiers

Type ID
Primary 10885403421983
Package 50885403421981

Customer Contacts