FDA UDI In Commercial Distribution 🇺🇸 United States

Cascade IOMAX

DI: 00840067102831 · Model: 199291-200 · CADWELL INDUSTRIES, INC.
Product Codes
10
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cascade IOMAX
Primary DI
00840067102831
Version / Model
199291-200
Company Name
CADWELL INDUSTRIES, INC.
Labeler DUNS
098554157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-10
Public Version
2
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
77fa1ed0-6d8b-4b75-8407-20c9bffe866e

Device Description

IOMAX EARPHONE INSERT CABLE

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
Yes
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
GZO Device, galvanic skin response measurement
IKN Electromyograph, diagnostic
ETN STIMULATOR, NERVE
DQA Oximeter
GWQ Full-montage Standard Electroencephalograph
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
GWE Stimulator, photic, evoked response
GWJ STIMULATOR, AUDITORY, EVOKED RESPONSE
JXE DEVICE, NERVE CONDUCTION VELOCITY MEASUREMENT
OLT Non-normalizing quantitative electroencephalograph software

GMDN Terms

Code Name
11474 Electromyograph

Identifiers

Type ID
Primary 00840067102831

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162199 000