FDA UDI In Commercial Distribution 🇺🇸 United States

Oximeter Plus

DI: 00860298000089 · Model: QuickCheck Pro · OXIMETER PLUS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oximeter Plus
Primary DI
00860298000089
Version / Model
QuickCheck Pro
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
3
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
1f9ac4f8-9957-4ff1-95e0-60a996b2ff93

Device Description

Fingertip Pulse Oximeter

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
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
OCH Oximeter, Infrared, Sporting, Aviation

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Primary 00860298000089

Customer Contacts

Phone
516-626-6226

Storage Conditions

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