FDA UDI In Commercial Distribution 🇺🇸 United States

Masimo Sensor

DI: 00843997016797 · Model: 4935 · MASIMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Masimo Sensor
Primary DI
00843997016797
Version / Model
4935
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
b58f9a99-5d50-4dbf-a0ce-5ef04b5ae7eb

Device Description

Masimo Sensor Replacement

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
No
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
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 00843997016797

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183697 000