Primary Device ID | 00817238010691 |
NIH Device Record Key | 6b1d6b26-9203-487f-87f2-96b6bb4939a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Protein 4 Calibration verifier Set for the Roche Integra |
Version Model Number | 98504 |
Company DUNS | 078742335 |
Company Name | CLINIQA CORPORATION |
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 | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817238010691 [Primary] |
JJY | Multi-Analyte Controls, All Kinds (Assayed) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-02-10 |
Device Publish Date | 2020-01-31 |
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