FDA UDI In Commercial Distribution 🇺🇸 United States

Sierra Wave

DI: 00840067101209 · Model: 190217-200 · CADWELL INDUSTRIES, INC.
Product Codes
8
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sierra Wave
Primary DI
00840067101209
Version / Model
190217-200
Company Name
CADWELL INDUSTRIES, INC.
Labeler DUNS
098554157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-05
Public Version
4
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
03c2d0ea-ca6f-4fb4-9704-7aec4ad817f1

Device Description

Sierra Wave Stimtroller

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
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
GWJ STIMULATOR, AUDITORY, EVOKED RESPONSE
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
GWQ Full-montage Standard Electroencephalograph
OLT Non-normalizing quantitative electroencephalograph software
GWE Stimulator, photic, evoked response
OLV Standard polysomnograph with electroencephalograph
IKN Electromyograph, diagnostic
JXE DEVICE, NERVE CONDUCTION VELOCITY MEASUREMENT

GMDN Terms

Code Name
11474 Electromyograph

Identifiers

Type ID
Primary 00840067101209

Customer Contacts