Primary Device ID | 20763000037509 |
NIH Device Record Key | 89df88f6-aa14-4aec-bdcb-50506e783da4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Microgel® |
Version Model Number | 1083303 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Lumen/Inner Diameter | 1.27 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000037505 [Primary] |
GS1 | 20763000037509 [Package] Contains: 00763000037505 Package: PK [50 Units] In Commercial Distribution |
ETD | TUBE, TYMPANOSTOMY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-14 |
Device Publish Date | 2020-09-06 |
20763000041315 | VENT TUBE 25443 50PK PAPA .040 SIL |
20763000040554 | VENT TUBE 25502 10PK ARMSTRONG PAIR 1.14 |
20763000040547 | VENT TUBE 25501 MICROGEL 5PK ARMSTG 1.14 |
20763000040523 | VENT TUBE 25441 MICROGEL 5PK PAPA 1.02 |
20763000037516 | VENT TUBE 1084401 5PK GROMMET 1.27 |
20763000037509 | VENT TUBE 1083303 50PK SHEEHY TYPE 1.27 |
20763000037486 | VENT TUBE 1083301 5PK SHEEHY TYPE 1.27 |
20763000037479 | VENT TUBE 1082203 50PK PAPA TYPE 1.14 |
20763000037462 | VENT TUBE 1082202 10PK PAPA TYPE PR 1.14 |
20763000037455 | VENT TUBE 1082201 5PK PAPA TYPE 1.14 |
20763000037431 | VENT TUBE 1081101 5PK ARMS MOD GROM 1.14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICROGEL 98454367 not registered Live/Pending |
Life Science Institute, LLC 2024-03-18 |
MICROGEL 97977708 not registered Live/Pending |
Bedding Acquisition, LLC 2022-06-14 |
MICROGEL 97456624 not registered Live/Pending |
Bedding Acquisition, LLC 2022-06-14 |
MICROGEL 87929741 not registered Live/Pending |
Life Science Institute, LLC 2018-05-21 |
MICROGEL 85694853 not registered Dead/Abandoned |
Elite Foam, Inc. 2012-08-03 |
MICROGEL 85393646 not registered Dead/Abandoned |
Zinus Inc. 2011-08-09 |
MICROGEL 85322122 4147789 Live/Registered |
Illinois Tool Works Inc. 2011-05-16 |
MICROGEL 78381520 2930924 Live/Registered |
FRIGEL FIRENZE S.P.A. 2004-03-10 |
MICROGEL 77949416 3915163 Dead/Cancelled |
Albaugh, Inc. 2010-03-03 |
MICROGEL 77228529 not registered Dead/Abandoned |
HEAD USA, Inc. 2007-07-12 |
MICROGEL 77017507 3273626 Live/Registered |
Medtronic Xomed, Inc. 2006-10-10 |
MICROGEL 75698867 2467012 Dead/Cancelled |
MicroStone Building Systems, LLC 1999-05-06 |