Primary Device ID | 00817089020191 |
NIH Device Record Key | 32498200-23e1-49c3-a334-d8396d47fd08 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Diazyme |
Version Model Number | DZ112B-CON |
Company DUNS | 080507219 |
Company Name | DIAZYME 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817089020191 [Primary] |
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 | 2016-11-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DIAZYME 76016954 2586200 Live/Registered |
General Atomics, Inc. 2000-04-03 |
DIAZYME 74344385 1800360 Live/Registered |
DANISCO US INC. 1992-12-30 |
DIAZYME 71147806 0172650 Live/Registered |
Takamine Laboratory, Inc. 1921-05-16 |