Primary Device ID | 00852553007025 |
NIH Device Record Key | 68823e77-00d1-4504-afc1-b57869a258f2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HDL Cholesterol Verifier Kit |
Version Model Number | 9560 |
Company DUNS | 189023351 |
Company Name | VERICHEM LABORATORIES, 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 | 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 |
Phone | 18005525859 |
customerservice@verichemlabs.com |
Total Volume | 30 Milliliter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852553007025 [Primary] |
JIS | Calibrator, Primary |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-29 |
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