Primary Device ID | 24714127866806 |
NIH Device Record Key | 6f004213-b46e-48a8-b03c-d72e12c44f24 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Unimax |
Version Model Number | FPS133059 |
Company DUNS | 658122465 |
Company Name | UNIMAX MEDICAL SYSTEMS INC. |
Device Count | 10 |
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 |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Outer Diameter | 5 Millimeter |
Length | 33 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04714127866802 [Unit of Use] |
GS1 | 14714127866809 [Primary] |
GS1 | 24714127866806 [Package] Contains: 14714127866809 Package: Carton [10 Units] In Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-18 |
Device Publish Date | 2021-08-10 |
14714127866236 | Monopolar Forceps |
24714127866806 | Monopolar spatula probe |
24714127866707 | Monopolar L hook probe |
24714127866608 | Monopolar J hook probe |
14714127868711 | Closed suction catheter |
14714127868568 | Closed suction catheter |
14714127868551 | Closed suction catheter |
14714127863570 | Detachable endo pocket |
14714127866007 | Monopolar Scissors |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UNIMAX 97633729 not registered Live/Pending |
AIYING DI 2022-10-15 |
UNIMAX 90468855 not registered Live/Pending |
Maher Fallaha 2021-01-15 |
UNIMAX 90160384 not registered Live/Pending |
Sunsation, Inc. 2020-09-04 |
UNIMAX 88840548 not registered Live/Pending |
Indorama Ventures Oxides LLC 2020-03-19 |
UNIMAX 87411830 5329056 Live/Registered |
DYNO NOBEL INC. 2017-04-14 |
UNIMAX 87389652 5311149 Live/Registered |
Biersch, Inc. 2017-03-28 |
UNIMAX 87292918 5358265 Live/Registered |
JOYETECH EUROPE HOLDING GMBH 2017-01-08 |
UNIMAX 86613292 not registered Dead/Abandoned |
CHIU, CHING-YEN 2015-04-29 |
UNIMAX 79225519 5624794 Live/Registered |
Mirka Ltd 2017-12-15 |
UNIMAX 79085942 4027611 Dead/Cancelled |
AVF Group Limited 2010-07-21 |
UNIMAX 79055863 3658237 Live/Registered |
KYODO YUSHI CO., LTD. 2008-06-18 |
UNIMAX 79020600 3251956 Dead/Cancelled |
KWH Mirka Ltd. 2005-03-29 |