Primary Device ID | 25060238200671 |
NIH Device Record Key | 0c214bde-3336-4da4-8d26-788a65960696 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HiVac™ Syringe Bone Cement Mixing and Delivery System |
Version Model Number | S727 |
Company DUNS | 221751311 |
Company Name | SUMMIT MEDICAL LIMITED |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15060238200674 [Primary] |
GS1 | 25060238200671 [Package] Contains: 15060238200674 Package: Carton [10 Units] In Commercial Distribution |
KIH | Dispenser, Cement |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-12-09 |
Device Publish Date | 2021-12-01 |
25060238200671 | Bone Cement Mixing and Delivery System |
25060238200336 | Bone Cement Mixing and Delivery System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HIVAC 76312288 2873143 Dead/Cancelled |
SUMMIT MEDICAL LIMITED 2001-09-14 |
HIVAC 74347705 not registered Dead/Abandoned |
WOODWARD-CLYDE CONSULTANTS 1993-01-12 |