FDA UDI In Commercial Distribution 🇺🇸 United States

CONTEC

DI: 06945040100515 · Model: CMS9000 · Contec Medical Systems Co., Ltd.
Product Codes
8
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONTEC
Primary DI
06945040100515
Version / Model
CMS9000
Company Name
Contec Medical Systems Co., Ltd.
Labeler DUNS
529606295
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
78de1b79-bc11-467d-a185-87ac29904889

Device Description

Patient Monitor

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZQ Monitor, Breathing Frequency
DQA Oximeter
DSK Computer, Blood-Pressure
DXN System, Measurement, Blood-Pressure, Non-Invasive
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MLD Monitor, St Segment With Alarm
DSI Detector And Alarm, Arrhythmia
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

GMDN Terms

Code Name
33586 General-purpose multi-parameter bedside monitor

Identifiers

Type ID
Primary 06945040100515

Premarket Submissions

Submission Number Supplement Number
K101692 000