Primary Device ID | 05407010126952 |
NIH Device Record Key | 1651aa21-86b6-485a-a999-e0dbad656d73 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NaCit 400, 6.0 - 500L Bag |
Version Model Number | BESP1711P500 |
Catalog Number | BESP1711P500 |
Company DUNS | 370158847 |
Company Name | Lonza Verviers |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 05407010126952 [Primary] |
PPM | General Purpose Reagent |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-22 |
Device Publish Date | 2025-05-14 |
05407010126938 - DPBS 0.0095M(PO4) w/o Ca,Mg-250ml sample | 2025-05-22 |
05407010126952 - NaCit 400, 6.0 - 500L Bag | 2025-05-22 |
05407010126952 - NaCit 400, 6.0 - 500L Bag | 2025-05-22 |
05407010126969 - TheraPEAK® T-VIVO® MEDIUM 5L BAG | 2025-05-22 |
05407010126921 - Powder 4 - 100L | 2025-05-20 |
05407010126877 - IMDM w/25mM HEPES wo PR or L-Gln 20L bag | 2025-05-08 |
05407010126884 - IMDM w/25mM HEPES wo PR or L-Gln, 1L | 2025-05-08 |
05407010126891 - NaP-56: 1000L Bag (empty bag capacity) | 2025-05-08 |
05407010126907 - NaP-56 : 200L Bag (empty bag capacity) | 2025-05-08 |