Primary Device ID | 04540217420537 |
NIH Device Record Key | e56decc5-04d6-47ad-9b6f-6ea4510323e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DGU-405 CL |
Version Model Number | 228-65019-55 |
Company DUNS | 690558747 |
Company Name | SHIMADZU CORPORATION |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04540217420537 [Primary] |
KIE | Apparatus, High Pressure Liquid Chromatography |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-01-25 |
Device Publish Date | 2021-01-15 |
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