Primary Device ID | 04054839076244 |
NIH Device Record Key | 460837b8-46ea-45b2-876b-ae6f52419a0b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Minicon B15 |
Version Model Number | 9031 |
Company DUNS | 896873994 |
Company Name | MERCK MILLIPORE LIMITED |
Device Count | 40 |
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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04054839076244 [Primary] |
GS1 | 04054839077913 [Unit of Use] |
JJH | Clinical Sample Concentrator |
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 | 2016-09-23 |
04053252359194 - Multiscreen-HTS HV | 2023-10-23 |
04053252466274 - Multiscreen-HTS HV | 2023-10-23 |
04053252504501 - Multiscreen-HV | 2023-10-23 |
04053252505928 - Multiscreen-HV | 2023-10-23 |
04061839736382 - Amicon Ultra – 15 | 2022-05-11 |
04061839736399 - Amicon Ultra – 4 | 2022-05-11 |
04061839736405 - Amicon Ultra – 15 | 2022-05-11 |
04061839736412 - Amicon Ultra – 4 | 2022-05-11 |