Primary Device ID | 00819704020036 |
NIH Device Record Key | c0331a83-8ffe-456f-a63b-fd3798274662 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Baebies |
Version Model Number | 0974 |
Catalog Number | 0974 |
Company DUNS | 079264306 |
Company Name | BAEBIES, INC. |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | (844) 244-4034 |
techsupport@baebies.com | |
Phone | (844) 244-4034 |
techsupport@baebies.com |
Storage Environment Temperature | Between -80 Degrees Celsius and -70 Degrees Celsius |
Storage Environment Temperature | Between -80 Degrees Celsius and -70 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00819704020036 [Primary] |
JJY | Multi-Analyte Controls, All Kinds (Assayed) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-01-18 |
00819704020210 | Quality Control Dried Blood Spot - Intermediate |
00819704020067 | Quality Control Dried Blood Spot - High |
00819704020050 | Quality Control Dried Blood Spot - Medium |
00819704020043 | Quality Control Dried Blood Spot - Low |
00819704020036 | Quality Control Dried Blood Spot - Base Pool |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BAEBIES 86580936 5005262 Live/Registered |
Baebies, Inc. 2015-03-30 |