Primary Device ID | 00816469021155 |
NIH Device Record Key | 9f9b0983-1cee-44c5-8f9d-27f90bd76896 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DS-600-PL |
Version Model Number | DS-600-PL |
Catalog Number | DS-600-PL |
Company DUNS | 177234754 |
Company Name | LASER PERIPHERALS, LLC |
Device Count | 1 |
DM Exempt | true |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00816469021155 [Primary] |
GEX | Powered laser surgical instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-06-20 |
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00816469021636 - DBSS-272-PL | 2022-05-30 272u Laser Fiber PL |
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00816469021599 - HTB-800 | 2021-03-30 800u Laser Fiber |