FDA UDI In Commercial Distribution 🇺🇸 United States

Alaris

DI: 10885403232541 · Model: 10011301 · BD Switzerland Sàrl
Product Codes
2
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
Primary DI
10885403232541
Version / Model
10011301
Catalog Number
10011301
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
5
Public Version Date
2023-06-07
Public Version Status
Update
Public Device Record Key
ad2d5203-be61-4a6a-9858-8ac27c6734fc

Device Description

Pump Infusion Set, Yellow-Striped Microbore Tubing Back Check Valve 302 cm (119 in)

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
LHI Set, i.V. Fluid transfer

GMDN Terms

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

Identifiers

Type ID
Primary 10885403232541
Package 50885403232549

Customer Contacts

Device Sizes

Type Value Unit Text
Length 119 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 125 Degrees Fahrenheit