Primary Device ID | 00810040255403 |
NIH Device Record Key | c28fdf05-bd5f-4f0c-a014-e225f33eaf7e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LED LIGHT SOURCE, A-SERIES, V2 |
Version Model Number | M A801-LEDV2 |
Company DUNS | 824793335 |
Company Name | GLOBAL SURGICAL CORPORATION |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810040255403 [Primary] |
EPT | Microscope, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-04 |
Device Publish Date | 2024-09-26 |
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00810040255403 - LED LIGHT SOURCE, A-SERIES, V2 | 2024-10-04 |
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