FDA UDI In Commercial Distribution 🇺🇸 United States

Masimo W1

DI: 00843997017503 · Model: 95080-104 · MASIMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Masimo W1
Primary DI
00843997017503
Version / Model
95080-104
Company Name
MASIMO CORPORATION
Labeler DUNS
780421038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-02
Public Version
1
Public Version Date
2024-03-11
Public Version Status
New
Public Device Record Key
0e3d9756-6792-48a8-a6f7-3a01d0cda4b7

Device Description

Masimo W1, Global, Switzerland

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
DPS Electrocardiograph

GMDN Terms

Code Name
65834 Wearable multiple vital physiological parameter monitoring system

Identifiers

Type ID
Primary 00843997017503

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K232512 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
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
0 – 35 Degrees Celsius