FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921839751 · Model: JL-900P · NIHON KOHDEN CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921839751
Version / Model
JL-900P
Catalog Number
JL-900P
Company Name
NIHON KOHDEN CORPORATION
Labeler DUNS
690568050
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-05
Public Version
5
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
9253d76d-08ba-4ef4-8348-7ca3cda716d4

Device Description

SpO2 connection cord (for Nihon Kohden SpO2 probe)

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
No
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
GWQ Full-montage Standard Electroencephalograph
MHX MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

GMDN Terms

Code Name
33586 General-purpose multi-parameter bedside monitor

Identifiers

Type ID
Primary 04931921839751

Customer Contacts