Primary Device ID | 00015482510077 |
NIH Device Record Key | 2023e2f6-5480-4acc-9cec-1898d9b593ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Assure® Control Level 3 Control Solution (High) |
Version Model Number | 510007 |
Company DUNS | 008171162 |
Company Name | ARKRAY USA, 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 | 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 | false |
OTC Over-The-Counter | true |
Phone | 1-800-566-8558 |
xxx@xxx.xxx |
Storage Environment Temperature | Between 36 Degrees Fahrenheit and 86 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00015482510077 [Primary] |
JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-09 |
Device Publish Date | 2019-04-01 |
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