FDA UDI In Commercial Distribution 🇺🇸 United States

RD

DI: 00843997016001 · Model: 9992 · MASIMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RD
Primary DI
00843997016001
Version / Model
9992
Company Name
MASIMO CORPORATION
Labeler DUNS
780421038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-16
Public Version
1
Public Version Date
2022-03-24
Public Version Status
New
Public Device Record Key
d79472be-b13d-43a8-a878-a82fad10d0b0

Device Description

RD Single-patient Use Conversion 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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter

GMDN Terms

Code Name
31658 Pulse oximeter probe, single-use

Identifiers

Type ID
Primary 00843997016001

Customer Contacts

Storage Conditions

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