Primary Device ID | 10842430106870 |
NIH Device Record Key | 58169a4f-f017-45cb-862f-b0cd2620ad1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COVER, 6" PERINEAL POST, DISPOSABLE |
Version Model Number | 5929 |
Catalog Number | 5929DZ |
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 | 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 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00842430106873 [Primary] |
GS1 | 10842430106870 [Package] Contains: 00842430106873 Package: [12 Units] In Commercial Distribution |
KME | Bedding, Disposable, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-18 |
Device Publish Date | 2019-01-18 |
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 |