HALF TRACK
GUDID 00842430107429
MIZUHO ORTHOPEDIC SYSTEMS, INC.
Patient transfer sliding mat| Primary Device ID | 00842430107429 |
| NIH Device Record Key | f0bceb3e-1dcc-44e3-b3f6-32e05b28445a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HALF TRACK |
| Version Model Number | 901 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 800-777-4764 |
| CustServ@mizuhosi.com | |
| Phone | 800-777-4764 |
| CustServ@mizuhosi.com | |
| Phone | 800-777-4764 |
| CustServ@mizuhosi.com | |
| Phone | 800-777-4764 |
| CustServ@mizuhosi.com | |
| Phone | 800-777-4764 |
| CustServ@mizuhosi.com | |
| Phone | 800-777-4764 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com | |
| Phone | 1-800-777-4674 |
| CustServ@mizuhosi.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842430107429 [Primary] |
FDA Product Code
| FMR | Device, Transfer, Patient, Manual |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-27 |
| Device Publish Date | 2022-05-19 |
Devices Manufactured by MIZUHO ORTHOPEDIC SYSTEMS, INC.
| 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 | 2025-08-05 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 |
Trademark Results [HALF TRACK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HALF TRACK 74493980 1959253 Dead/Cancelled |
Arner, Barbara D. 1994-02-24 |
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