FDA UDI In Commercial Distribution 🇺🇸 United States

Radius-7

DI: 00843997010047 · Model: 4196 · MASIMO CORPORATION
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
Radius-7
Primary DI
00843997010047
Version / Model
4196
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
2
Public Version Date
2023-03-14
Public Version Status
Update
Public Device Record Key
9e962ece-e552-4cea-b604-8041fc348de3

Device Description

Radius-7 Wearable Instrument

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
Yes
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 00843997010047
Direct Marking 00843997015875

Customer Contacts

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius