FDA UDI In Commercial Distribution 🇺🇸 United States

Masimo

DI: 00843997016605 · Model: 9783 · MASIMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Masimo
Primary DI
00843997016605
Version / Model
9783
Company Name
MASIMO CORPORATION
Labeler DUNS
780421038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-08
Public Version
1
Public Version Date
2021-10-18
Public Version Status
New
Public Device Record Key
c6d5a073-1670-4062-9a7b-50f15a1989c9

Device Description

Kit, Rad-97, Homecare

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWI Monitor, physiological, patient (without arrhythmia detection or alarms)

GMDN Terms

Code Name
46201 Pulse Co-oximeter

Identifiers

Type ID
Primary 00843997016605

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
15 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius