Primary Device ID | 00664816003664 |
NIH Device Record Key | 870a26f8-1db9-4f15-97fa-a70944337ccc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LW Scientifc, Inc |
Version Model Number | CPL-FXDR-05S3 |
Catalog Number | CPL-FXDR-05S3 |
Company DUNS | 785335381 |
Company Name | LW SCIENTIFIC, INC. |
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 | true |
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 | 00664816003664 [Primary] |
IEG | Table, Slide Warming |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-06-08 |
Device Publish Date | 2020-05-31 |
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