Primary Device ID | 10628429001742 |
NIH Device Record Key | f4b983ad-e9bf-4827-bf8d-d58d373ffcf3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Legionella DFA Mounting Medium |
Version Model Number | PL.213 |
Catalog Number | PL.213 |
Company DUNS | 960418395 |
Company Name | PRO-LAB, INCORPORATED |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10628429001742 [Primary] |
LHL | Reagents, Antibody, Legionella, Direct & Indirect Fluorescent |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-07-25 |
Device Publish Date | 2022-12-25 |
10628429001742 - Legionella DFA Mounting Medium | 2024-07-25 Mounting Medium |
10628429001742 - Legionella DFA Mounting Medium | 2024-07-25 Mounting Medium |
00817978020004 - Vision 2 | 2018-03-29 Salmonella O Polyvalent A-I Kit Group: A, B, C, D, E, F, G, H, I |
00817978020011 - Vision 2 | 2018-03-29 Salmonella OMA Group: A, B, C, D, E, L |
00817978020028 - Vision 2 | 2018-03-29 Salmonella OMB Group: C, F, G, H |
00817978020035 - Vision 2 | 2018-03-29 Salmonella OMC Group: I, J, K, M, N, O, P |
00817978020073 - Vision 2 | 2018-03-29 Salmonella OMD Group: Q, R, S, T, U, V, W |
00817978020080 - Vision 2 | 2018-03-29 Salmonella OME Group: X, Y,Z, 51, 52, 53, 61 |
00817978020097 - Vision 2 | 2018-03-29 Salmonella OMF Group: 54, 55, 56, 57, 58, 59 |