Primary Device ID | 00852553007070 |
NIH Device Record Key | e4d4b4a8-d646-46eb-b2d3-5ea3b7a1ecf3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bilirubin Standard, Level F |
Version Model Number | 9436 |
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 | 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 | false |
Phone | 18005525859 |
customerservice@gmail.com |
Total Volume | 10 Milliliter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852553007070 [Primary] |
JIT | Calibrator, Secondary |
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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00852553007070 - Bilirubin Standard, Level F | 2018-07-06Calibrator / Calibration Verifier |
00852553007070 - Bilirubin Standard, Level F | 2018-07-06 Calibrator / Calibration Verifier |