FDA UDI In Commercial Distribution 🇺🇸 United States

Alaris

DI: 10885403822018 · Model: 8220 · CAREFUSION 303, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Alaris
Primary DI
10885403822018
Version / Model
8220
Company Name
CAREFUSION 303, INC.
Labeler DUNS
360624720
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
347ff988-c76b-4ff5-852e-597ae14e177c

Device Description

Alaris SP02 Module Massimo

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter

GMDN Terms

Code Name
36554 Patient monitoring system module, pulse oximetry

Identifiers

Type ID
Primary 10885403822018

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010966 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
5 – 85 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Storage Environment Atmospheric Pressure 760 Low to 375 High mmHg