Primary Device ID | 00840067100530 |
NIH Device Record Key | dc362646-4127-4a74-835d-2fa6a762928f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sierra Wave |
Version Model Number | 199220-200 |
Company DUNS | 098554157 |
Company Name | CADWELL INDUSTRIES, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com | |
Phone | +1(509)735-6481 |
applications@cadwell.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840067100530 [Primary] |
GWJ | STIMULATOR, AUDITORY, EVOKED RESPONSE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-14 |
Device Publish Date | 2016-09-05 |
00840067102046 | Skin Temperature Probe |
00840067102039 | Sierra Wave Footswitch |
00840067101209 | Sierra Wave Stimtroller |
00840067100769 | Amp-Stim Switch Box |
00840067100547 | SII Bone Vibrator |
00840067100530 | Light Weight Headphones |
00840067100523 | Acoustic Shielded Headphones |
00840067100516 | Cascade VEP/LED Goggles |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SIERRA WAVE 87914064 not registered Live/Pending |
Mammoth Beers, Inc. 2018-05-09 |
SIERRA WAVE 85417103 4235097 Live/Registered |
Aervoe Industries, Inc. 2011-09-07 |
SIERRA WAVE 78764268 3158582 Live/Registered |
BENETT KESSLER II TRUST 2005-12-01 |
SIERRA WAVE 76403566 2789577 Live/Registered |
Cadwell Industries, Inc. 2002-05-03 |