Primary Device ID | 00606959058453 |
NIH Device Record Key | d2a6eb5c-b62e-4cf4-90f5-9ff5004d6c49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SIMPLYGO |
Version Model Number | FR1113604 |
Catalog Number | FR1113604 |
Company DUNS | 080728314 |
Company Name | Respironics, Inc. |
Device Count | 1 |
DM Exempt | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00606959058453 [Primary] |
CAW | Generator, oxygen, portable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-06 |
Device Publish Date | 2020-06-26 |
00606959048812 | SIMPLYGO,INTERNATIONAL, IT |
00606959028852 | SimplyGo, Saudi Arabia |
00606959058453 | SimplyGo Mini, Standard Battery, France |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SIMPLYGO 97681749 not registered Live/Pending |
Social Media, LLC 2022-11-17 |
SIMPLYGO 86402500 4965419 Live/Registered |
SimplyShe, Inc. 2014-09-22 |
SIMPLYGO 79114857 4378118 Live/Registered |
Koninklijke Philips N.V. 2012-06-01 |