FDA UDI In Commercial Distribution 🇺🇸 United States

Radius PPG

DI: 00843997014779 · Model: 9954 · MASIMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Radius PPG
Primary DI
00843997014779
Version / Model
9954
Company Name
MASIMO CORPORATION
Labeler DUNS
780421038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-16
Public Version
2
Public Version Date
2021-01-18
Public Version Status
Update
Public Device Record Key
d189b4c8-aab5-4a02-8afd-e7ed440c2002

Device Description

Radius PPG Kit, Adt Tetherless Pulse Oximetry Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter

GMDN Terms

Code Name
46201 Pulse Co-oximeter

Identifiers

Type ID
Primary 00843997014779

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183697 000

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
0 – 50 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity