Primary Device ID | 03770025849089 |
NIH Device Record Key | 9d4accba-56fb-4b26-b531-62059087e434 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maestro Couplers, 5mm |
Version Model Number | 200 |
Company DUNS | 117926846 |
Company Name | Moon Surgical Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 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 | 03770025849089 [Primary] |
FQO | Table, Operating-Room, Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-09 |
Device Publish Date | 2024-10-01 |
03770025849072 - Maestro Couplers, 10mm | 2024-10-09 |
03770025849089 - Maestro Couplers, 5mm | 2024-10-09 |
03770025849089 - Maestro Couplers, 5mm | 2024-10-09 |
03770025849096 - Maestro System | 2024-09-11 The Maestro System is intended to hold and position laparoscopes and laparoscopic instruments during laparoscopic surgical proce |