miniARM® multiSTATION™ System 081581
GUDID 00850012846321
BITA RetroSterno™ Paddle
LSI Solutions, Inc.
Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable| Primary Device ID | 00850012846321 |
| NIH Device Record Key | 6ebd7aa3-dc89-4348-af0a-0973bd1a61ad |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | miniARM® multiSTATION™ System |
| Version Model Number | 081581 |
| Catalog Number | 081581 |
| Company DUNS | 603420183 |
| Company Name | LSI Solutions, 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com | |
| Phone | +1(866)575-3493 |
| regulatorydpt@lsisolutions.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850012846321 [Primary] |
FDA Product Code
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
[00850012846321]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-11 |
| Device Publish Date | 2024-01-03 |
On-Brand Devices [miniARM® multiSTATION™ System]
| 00850012846185 | RetroSterno™ PADDLE KIT (1 each LIMA and RIMA RetroSterno™ Paddle) |
| 00850012846178 | RIMA RetroSterno™ PADDLE |
| 00850012846161 | LIMA RetroSterno™ PADDLE |
| 00850012846154 | SubX™ STERNAL ASCENDER™ SYSTEM |
| 00850012846147 | M55™ RIGID miniARM® HOLDER |
| 00850012846321 | BITA RetroSterno™ Paddle |
Trademark Results [miniARM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MINIARM 88239202 5870228 Live/Registered |
LSI Solutions, Inc. 2018-12-21 |
 MINIARM 87561608 not registered Dead/Abandoned |
LSI Solutions, Inc. 2017-08-09 |
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