Primary Device ID | 06976323220101 |
NIH Device Record Key | eb183d46-0550-49c2-b5be-aa3b9fbc5122 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STEREX |
Version Model Number | HOFF1000 |
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 | 06976323220101 [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 |