Primary Device ID | 04527799700097 |
NIH Device Record Key | 3c8e25c0-a7e8-4b19-a854-adafd27c9112 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Linking Arm |
Version Model Number | KC-0582U |
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 | false |
Serial Number | false |
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 | 04527799700097 [Primary] |
FOX | Stand, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-16 |
Device Publish Date | 2024-07-08 |
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