Primary Device ID | 04049188060013 |
NIH Device Record Key | b2502507-7b66-4bb1-bba3-660c5f63a6ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Heatable reagent st. kit |
Version Model Number | 000000014047534612 |
Catalog Number | 14047534612 |
Company DUNS | 315539452 |
Company Name | Leica Biosystems Nussloch GmbH |
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 | 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 | false |
OTC Over-The-Counter | true |
Phone | +4962241430 |
chs.support@leicabiosystems.co |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 * |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049188060013 [Primary] |
KPA | Slide stainer, automated |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-01-04 |
Device Publish Date | 2018-12-04 |
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