FDA UDI In Commercial Distribution 🇺🇸 United States

oximeter - RO2

DI: 00382098017062 · Model: 1 · Raya Pharmaceuticals LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
oximeter - RO2
Primary DI
00382098017062
Version / Model
1
Company Name
Raya Pharmaceuticals LLC
Labeler DUNS
106631637
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-31
Public Version
1
Public Version Date
2024-11-08
Public Version Status
New
Public Device Record Key
6797ef4f-8ec9-4b77-8802-2a2fc381db50

Device Description

The pulse oximeter is a reusable device and intended for spot-checking of oxygen saturation and pulse rate for use with the finger of adult patients in healthcare environments. And it is not intended to be used under motion or low perfusion scenarios.

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
Yes
Has Manufacturing Date
No
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
37808 Pulse oximeter probe, reusable

Identifiers

Type ID
Primary 00382098017062

Premarket Submissions

Submission Number Supplement Number
K191430 000