Primary Device ID | 10847399017243 |
NIH Device Record Key | f38ef4d9-c6ec-4e8a-a0f1-d55188a68f44 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroAire® |
Version Model Number | 83030-1 |
Catalog Number | 83030-6 |
Company DUNS | 103056420 |
Company Name | Microaire Surgical Instruments LLC |
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 | 00847399017246 [Primary] |
GS1 | 10847399017243 [Package] Contains: 00847399017246 Package: PK [6 Units] In Commercial Distribution |
EMF | Knife, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-23 |
Device Publish Date | 2022-06-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICROAIRE 85293147 4028959 Live/Registered |
MicroAire Surgical Instruments, LLC 2011-04-12 |
MICROAIRE 85293112 4028958 Live/Registered |
MicroAire Surgical Instruments, LLC 2011-04-12 |
MICROAIRE 77669900 3676034 Live/Registered |
MicroAire Surgical Instruments, LLC 2009-02-13 |
MICROAIRE 76599958 3091920 Live/Registered |
MicroAire Surgical Instruments LLC 2004-06-30 |
MICROAIRE 75382346 not registered Dead/Abandoned |
Housley, Todd B. 1997-10-31 |
MICROAIRE 74230956 1717856 Dead/Cancelled |
MICROAIRE SURGICAL INSTRUMENTS LLC 1991-12-13 |
MICROAIRE 73162923 1121370 Live/Registered |
AMERICAN SAFETY EQUIPMENT CORPORATION 1978-03-20 |