Primary Device ID | 04015630971114 |
NIH Device Record Key | f0b10a9e-eedc-4ce6-9238-e0a928277760 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LCS (Predilute) |
Version Model Number | 05264839001 |
Catalog Number | 05264839001 |
Company DUNS | 184042521 |
Company Name | Ventana Medical Systems, Inc. |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04015630971114 [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 | 2025-07-15 |
Device Publish Date | 2025-07-07 |
04015630971114 - LCS (Predilute) | 2025-07-15 |
04015630971114 - LCS (Predilute) | 2025-07-15 |
04015630976867 - ASSY,Reag.Disp.Card,PrepKit 18,BenchMark | 2025-07-15 |
04015630984299 - CINtec p16 Histology (50) CE | 2025-07-15 |
07613336100981 - ASSY,Reag.Disp.Card,PrepKit 13,BenchMark | 2025-07-15 |
07613336100998 - ASSY,Reag.Disp.Card,PrepKit 14,BenchMark | 2025-07-15 |
07613336101001 - ASSY,Reag.Disp.Card,PrepKit 4,BenchMark | 2025-07-15 |
07613336101018 - ASSY,Reag.Disp.Card,PrepKit 100,BenchMar | 2025-07-15 |
07613336101179 - NexES Dispenser Card Counterstain 1 | 2025-07-15 |