Primary Device ID | 01816835022037 |
NIH Device Record Key | 22138cc3-a06f-48da-925a-05eece7a826e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SYSTEM TWO LES |
Version Model Number | SD2CD2 |
Company DUNS | 093357739 |
Company Name | MEDICAL ILLUMINATION INTERNATIONAL INC. |
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 | 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 | 00816835022038 [Primary] |
GS1 | 01816835022037 [Package] Contains: 00816835022038 Package: BOX [1 Units] In Commercial Distribution |
FST | Light, Surgical, Fiberoptic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2019-08-01 |
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