Primary Device ID | 20898021000055 |
NIH Device Record Key | 59672136-1223-42f7-823e-6c6922042b93 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Alcavis 50 |
Version Model Number | 500 mL |
Catalog Number | 15501 |
Company DUNS | 078843940 |
Company Name | ANGELINI PHARMA 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00898021000051 [Primary] |
GS1 | 20898021000055 [Package] Contains: 00898021000051 Package: case [12 Units] In Commercial Distribution |
KDJ | Set, Administration, For Peritoneal Dialysis, Disposable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2016-08-29 |
20898021000062 | Electrolytic chloroxidizer high level disinfectant. |
20898021000055 | Electrolytic Chloroxidizer High Level Disinfectant. |
00898021000044 | Electrolytic Chloroxidizer High Level Disinfectant. |