FDA UDI In Commercial Distribution 🇺🇸 United States

O3

DI: 00843997013468 · Model: 4431 · MASIMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
O3
Primary DI
00843997013468
Version / Model
4431
Company Name
MASIMO CORPORATION
Labeler DUNS
780421038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-03
Public Version
2
Public Version Date
2021-01-18
Public Version Status
Update
Public Device Record Key
a2ed70e9-efb0-4995-aa5c-c12de033b339

Device Description

O3 Regional Oximeter, Philips

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
MUD Oximeter, tissue saturation

GMDN Terms

Code Name
17942 Cerebral oximeter

Identifiers

Type ID
Primary 00843997013468

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182429 000