FDA UDI In Commercial Distribution 🇺🇸 United States

Sierra Wave

DI: 00840067100547 · Model: 199224-200 · CADWELL INDUSTRIES, INC.
Product Codes
8
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sierra Wave
Primary DI
00840067100547
Version / Model
199224-200
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
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
9dabfa05-fb45-49ba-aaee-410eab90d675

Device Description

SII Bone Vibrator

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

GMDN Terms

Code Name
11474 Electromyograph

Identifiers

Type ID
Primary 00840067100547

Customer Contacts