Primary Device ID | 04527799705993 |
NIH Device Record Key | ba1caeae-8e83-486f-9797-7152daaa5497 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sittan |
Version Model Number | KF-890UW |
Company DUNS | 690552500 |
Company Name | PARAMOUNT BED 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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04527799705993 [Primary] |
IKX | Aid, Transfer |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-30 |
Device Publish Date | 2024-08-22 |
04527799700110 | Mechanical table to support a patient with the right position |
04527799705993 | Mechanical table to support a patient with the right position |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SITTAN 88758156 not registered Live/Pending |
Paramount Bed Company Limited 2020-01-14 |