Primary Device ID | 00849832010425 |
NIH Device Record Key | e016b443-8bd7-4592-8923-7c1f4e2e0166 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Leica Biosystems Ariol DM6000 B for Ariol PL200 Refurbished |
Version Model Number | 23MIC1206R |
Company DUNS | 082930884 |
Company Name | Leica Biosystems Richmond, 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 | 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 |
Phone | +1(800)5374669 |
tech.support@Leicabiosystems.com |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 * |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00849832010425 [Primary] |
NQN | MICROSCOPE,AUTOMATED,IMAGE ANALYSIS,IMMUNOHISTOCHEMISTRY,OPERATOR INTERVENTION,NUCLEAR INTENSITY & PERCENT POSITIVITY |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-17 |
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