FDA UDI In Commercial Distribution 🇺🇸 United States

TM-Oxi System

DI: B322B0011 · Model: B001 · LD TECHNOLOGY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TM-Oxi System
Primary DI
B322B0011
Version / Model
B001
Company Name
LD TECHNOLOGY, LLC
Labeler DUNS
079443785
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-16
Public Version
3
Public Version Date
2024-04-17
Public Version Status
Update
Public Device Record Key
c3d26ae8-c4a8-4028-9a53-5660e13d790c

Device Description

"Oxi-W system is intended for use: To spot check or monitor Oxygen saturation of arterial hemoglobin (SpO2%) and pulse rate. To analyze the pulse waveform (Photoplethysmography or PTG) provided by the oximeter. It only provides mathematical analysis of the input of the PTG using the first and second derivatives of the PTG values related to the microvascular condition. To analyze the basic rhythms of the NN or RR intervals in heart rate from the PTG, both in the time domain and in the frequency domain (short time 5 minutes). It only provides mathematical analysis of the heart rate variability values related to the autonomic nervous system function."

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

GMDN Terms

Code Name
16174 Manual-inflation electronic sphygmomanometer, non-portable

Identifiers

Type ID
Primary B322B0011

Customer Contacts

Phone
305-379-9900