Primary Device ID | B06711009000 |
NIH Device Record Key | dc404f6f-24b7-4102-83b2-a879049964cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LASE Accessory Kit |
Version Model Number | 1100-900 |
Catalog Number | 1100-900 |
Company DUNS | 010316284 |
Company Name | CLARUS MEDICAL, LLC |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Phone | 763-525-8400 |
admin@clarus-medical.com | |
Phone | 763-525-8400 |
admin@clarus-medical.com |
Storage Environment Temperature | Between -18 Degrees Celsius and 52 Degrees Celsius |
Storage Environment Temperature | Between -18 Degrees Celsius and 52 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B06711009000 [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 | 2016-09-22 |
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