| Primary Device ID | 06976323220118 |
| NIH Device Record Key | b8b33b9a-d386-487c-a10d-f685cba4654b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STEREX |
| Version Model Number | HOFF750SCALE |
| Company DUNS | 543064202 |
| Company Name | Jiangmen Jia Mei Medical Products Co., Ltd. |
| 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 | 06976323220118 [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 | 2024-01-31 |
| Device Publish Date | 2024-01-23 |
| 06976323220118 | HOFF750SCALE |
| 06976323220101 | HOFF1000 |
| 06976323220095 | HOFF750 |
| 06976323220088 | HOFF650 |
| 06976323220071 | HOFF500 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() STEREX 85031674 4033509 Dead/Cancelled |
TRI-STATE SURGICAL SUPPLY & EQUIPMENT LTD. 2010-05-06 |
![]() STEREX 79377631 not registered Live/Pending |
Wintersteiger AG 2023-06-13 |
![]() STEREX 75609616 not registered Dead/Abandoned |
SteriGenics International, Inc. 1998-12-21 |
![]() STEREX 73727507 1521666 Live/Registered |
E.A. ELLISON & COMPANY LIMITED 1988-05-09 |