Primary Device ID | 10813040013070 |
NIH Device Record Key | 9229adc6-9872-40ac-ab94-735dfc0580d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Power Cord for VS3 Cart - US |
Version Model Number | VS3 |
Catalog Number | 560-6669 |
Company DUNS | 532199478 |
Company Name | VISIONSENSE LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 10813040013070 [Primary] |
GWG | Endoscope, Neurological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-09-09 |
Device Publish Date | 2019-11-25 |
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