Primary Device ID | 06973134772102 |
NIH Device Record Key | 492d0087-746a-4ad8-ba0f-6bcdaaf7b653 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | silverfox |
Version Model Number | FD-2100 |
Company DUNS | 529252597 |
Company Name | Silverfox Corporation Limited |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973134772102 [Primary] |
CCQ | Nebulizer, Medicinal, Non-Ventilatory (Atomizer) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-22 |
Device Publish Date | 2023-12-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SILVERFOX 97442462 not registered Live/Pending |
SILVERFOX CORPORATION LIMITED 2022-06-03 |
SILVERFOX 97442428 not registered Live/Pending |
SILVERFOX CORPORATION LIMITED 2022-06-03 |
SILVERFOX 97442390 not registered Live/Pending |
SILVERFOX CORPORATION LIMITED 2022-06-03 |
SILVERFOX 90031432 not registered Live/Pending |
Divine Rejuvenation 2020-07-01 |
SILVERFOX 88716062 not registered Live/Pending |
Silverfox Management Group Pty Ltd 2019-12-05 |
SILVERFOX 87491318 5375359 Live/Registered |
Silver Fox Productions, Inc. 2017-06-15 |
SILVERFOX 78133969 2717606 Live/Registered |
HME, Incorporated 2002-06-07 |