| Primary Device ID | 05060433600777 |
| NIH Device Record Key | 2cec63f0-67c5-4a8e-a1c8-3e07406ff152 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LSSS |
| Version Model Number | RM04051 |
| Catalog Number | RM04051 |
| Company DUNS | 211167885 |
| Company Name | Lockdown Medical Ltd |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060433600777 [Primary] |
| MDM | Instrument, Manual, Surgical, General Use |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
[05060433600777]
High-level Disinfectant;Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-03 |
| Device Publish Date | 2020-07-24 |
| 05060433600715 | Lockdown Loop Tensioner - Single Use |
| 05060433600708 | Lockdown Angled Introducer for use on left shoulder - single use |
| 05060433600692 | Lockdown Angled Intrducer for use on right shoulder - single use |
| 05060433600920 | Lockdown (LSSS) Surgical Instrument Metal Tray Lid. This Tray lid attaches to the Lockdown Tray |
| 05060433600913 | DEPTH GAUGE INNER BODY WITH BALL & SPRING. THIS INNER TUBE HAS MARKINGS ON IT. IT SITS INSIDE TH |
| 05060433600906 | DEPTH GAUGE OUTER BODY TUBE. THIS TUBE HOUSES THE "DEPTH GAUGE INNER BODY WITH BALL & SPRING - |
| 05060433600890 | DEPTH GAUGE OUTER BODY CAP. THIS CAP SCREWS ONTO "DEPTH GAUGE OUTER BODY TUBE - RM06008 (DI NO# |
| 05060433600883 | AO SCREWDRIVER SPINNER (THIS PART FITS ONTO THE BOTTOM END OF "AO CANULATED SILICONE SCREWDRIVER |
| 05060433600876 | AO CANNULATED SILICONE SCREWDRIVER HANDLE WITH QUICK COUPLING. THE "AO SCREWDRIVER SPINNER" - DI |
| 05060433600845 | LOCKDOWN (LSSS) SURGICAL TRAY BASE WHICH HOUSES ALL INSTRUMENTS REQUIRED FOR THE LOCKDOWN SHOULD |
| 05060433600807 | DRILL SLEEVE Ø2.5mm & TAP SLEEVE Ø3.5mm. THE FINISHED PART NUMBER IS IN631/1 - "DRILL SLEEVE à |
| 05060433600777 | AO SCREWDRIVER SHAFT Ø2.5MM (HEX). THE FINISHED PART NUMBER IS IN629/1 - "AO SCREWDRIVER SHAFT |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LSSS 86890941 not registered Dead/Abandoned |
LockDown Medical Limited 2016-01-29 |