Primary Device ID | 00842430109157 |
NIH Device Record Key | c71aa12d-56c4-418a-81b4-942d8894ad75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ADANTE KNEE PROCEDURE KIT, RIGHT |
Version Model Number | 6895K-R |
Catalog Number | 6895K-R |
Company DUNS | 084527241 |
Company Name | MIZUHO ORTHOPEDIC 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 | 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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
00842430109140 - ADANTE KNEE PROCEDURE KIT, LEFT | 2025-08-05 Contains 6895TKA-L-CS Adante Knee Drape System, Left (case of 5) and 6895-75-5 Adante Knee Protection Kit (case of 5) |
00842430109157 - ADANTE KNEE PROCEDURE KIT, RIGHT | 2025-08-05Contains 6895TKA-L-CS Adante Knee Drape System, Right (case of 5) and 6895-75-5 Adante Knee Protection Kit (case of 5) |
00842430109157 - ADANTE KNEE PROCEDURE KIT, RIGHT | 2025-08-05 Contains 6895TKA-L-CS Adante Knee Drape System, Right (case of 5) and 6895-75-5 Adante Knee Protection Kit (case of 5) |
00842430109164 - ADANTE DAA HIP PROCEDURE KIT, LEFT | 2025-08-05 Contains 6895THA-L-CS Adante DAA-THA Drape, Left (case of 5) and 6895-76-5 Adante Hip Protection Kit (case of 5) |
00842430109171 - ADANTE DAA HIP PROCEDURE KIT, RIGHT | 2025-08-05 Contains 6895THA-R-CS Adante DAA-THA Drape, Right (case of 5) and 6895-76-5 Adante Hip Protection Kit (case of 5) |
00842430116728 - TRAPEZE ARM ASSEMBLY, PATIENT HELPER | 2025-08-05 |
00842430116261 - KIT, HANA SSXT MAQUET 1140 VERSION | 2025-01-20 |
10842430111539 - PKIT, INDIV W/SHEARGARD, SST-3000 (1) | 2024-05-20 |
00842430116322 - AQUARI IMMERSION CONTROLLER REFURB | 2024-03-15 |