| Primary Device ID | 06973134770139 |
| NIH Device Record Key | 8ff15a72-c771-4ada-aa73-e975c4c426d4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | silverfox |
| Version Model Number | NGO 303 (70 Density) |
| 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 | 06973134770139 [Primary] |
| FNL | Bed, Ac-Powered Adjustable Hospital |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-20 |
| Device Publish Date | 2023-12-12 |
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 |