FDA UDI In Commercial Distribution 🇺🇸 United States

Oximeter Plus

DI: 00860298000010 · Model: C21 · OXIMETER PLUS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oximeter Plus
Primary DI
00860298000010
Version / Model
C21
Company Name
OXIMETER PLUS, INC.
Labeler DUNS
829005607
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-04
Public Version
4
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
10709ee1-212b-415b-ab48-14dde69ac136

Device Description

Fingertip Pulse Oximeter

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
DQA Oximeter

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Primary 00860298000010

Customer Contacts

Phone
516-626-6226

Premarket Submissions

Submission Number Supplement Number
K161560 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-13 – 158 Degrees Fahrenheit