Primary Device ID | 00816879023091 |
NIH Device Record Key | b4b94db6-ef4a-4e0a-80c6-4049dabdaefb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NOVEOS Substrate Mix Container Pack |
Version Model Number | 118877-001 |
Company DUNS | 010558476 |
Company Name | HYCOR BIOMEDICAL LLC |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816879023091 [Primary] |
DHB | System, Test, Radioallergosorbent (Rast) Immunological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-01-19 |
Device Publish Date | 2021-01-11 |