Primary Device ID | 00810040250101 |
NIH Device Record Key | ba047d00-0516-40a2-b1d4-df64d3871604 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LED ILLUMINATION MODULE WITH COMPOSITE FILTER, PROTEGE SERIES, INTERNATIONAL |
Version Model Number | M 800PCF-I |
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 | true |
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 |