Microtek™ 9604UK
GUDID 30748426074946
Camera Cover
Microtek Medical Inc.
Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use| Primary Device ID | 30748426074946 |
| NIH Device Record Key | 2bfa4204-d220-4a40-ba92-cbcf5192dc52 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Microtek™ |
| Version Model Number | 9604UK |
| Catalog Number | 9604UK |
| Company DUNS | 106908437 |
| Company Name | Microtek Medical 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00748426074945 [Primary] |
| GS1 | 30748426074946 [Package] Contains: 00748426074945 Package: [25 Units] In Commercial Distribution |
| GS1 | 50748426074940 [Package] Contains: 00748426074945 Package: [25 Units] In Commercial Distribution |
FDA Product Code
| PUI | Drape, Surgical, Exempt |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
[30748426074946]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-29 |
| Device Publish Date | 2022-09-21 |
Devices Manufactured by Microtek Medical Inc.
| 50748426113748 - Ecolab | 2023-12-08 CoreTemp Fluid Warmer |
| 50748426126731 - Ecolab | 2023-11-24 Hush Slush 2.0 Ecolab Slush & Warmer System |
| 08425921000502 - MICROTEK | 2023-03-22 7Day,Sterile,TapFilter,w/ SprayOutlet (1) |
| 18425921000530 - MICROTEK | 2023-03-22 7Day,Sterile,TapFilter,w/ SprayOutlet (1) |
| 18425921000578 - MICROTEK | 2023-03-22 7Day,Sterile,TapFilter,w/ SprayOutlet (1) |
| 18425921000592 - MICROTEK | 2023-03-22 7Day,Sterile,TapFilter,w/ SprayOutlet (1) |
| 18425921000615 - MICROTEK | 2023-03-22 7Day,Sterile,TapFilter,w/ SprayOutlet (1) |
| 18425921000639 - MICROTEK | 2023-03-22 7Day,Sterile,TapFilter,w/ SprayOutlet (1) |
Trademark Results [Microtek]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MICROTEK 88301892 not registered Live/Pending |
Fusion Optix, Inc. 2019-02-14 |
 MICROTEK 87633574 5496159 Live/Registered |
SYNATEK LP 2017-10-04 |
 MICROTEK 86919715 5216223 Live/Registered |
Fleurco Products Inc. 2016-02-25 |
 MICROTEK 77263723 not registered Dead/Abandoned |
United States Liability Insurance Company and its affiliates 2007-08-24 |
 MICROTEK 76572201 2924836 Live/Registered |
MICROTEK MEDICAL, INC. 2004-01-23 |
 MICROTEK 76512696 2852990 Dead/Cancelled |
Kaydon Acquisition XI, Inc. 2003-05-08 |
 MICROTEK 75606937 not registered Dead/Abandoned |
Marburger Packing 1998-12-17 |
 MICROTEK 75555278 2494685 Dead/Cancelled |
SEALY TECHNOLOGY, LLC 1998-09-18 |
 MICROTEK 75387572 2277271 Live/Registered |
Microtek International Inc. 1997-11-10 |
 MICROTEK 73754327 not registered Dead/Abandoned |
MESSAGETECH PTY LIMITED 1988-09-22 |
 MICROTEK 73500210 1339096 Live/Registered |
Broan Mfg. Co., Inc. 1984-09-20 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.