FDA UDI In Commercial Distribution 🇺🇸 United States

Fingertip Pulse Oximeter

DI: 07540195054004 · Model: 01MN1000 · O-Two Medical Technologies Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Fingertip Pulse Oximeter
Primary DI
07540195054004
Version / Model
01MN1000
Catalog Number
01MN1000
Company Name
O-Two Medical Technologies Inc
Labeler DUNS
206449154
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
aed30418-1752-498e-8e62-deff527ac2b1

Device Description

Fingertip Pulse Oximeter is a portable non-invasive, spot-check, oxygen saturation of arterial hemoglobin (SpO2) and pulse rate of adult and pediatric patient at home, and hospital (including clinical use and in internist/surgery, Anesthesia, intensive care and etc.). Not for continuously monitoring.

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 07540195054004
Package 17540195054001

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070371 000

Device Sizes

Type Value Unit Text
Weight 28 Gram
Height 32 Millimeter
Width 34 Millimeter
Length 58 Millimeter

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 80 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius