MicroLink ASB-DG
GUDID 30845854648524
MICROLINK, CMC DRILL GUIDE
Conmed Corporation
Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable| Primary Device ID | 30845854648524 |
| NIH Device Record Key | 2783533f-794e-46cf-8c1e-64b413e3731c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MicroLink |
| Version Model Number | ASB-DG |
| Catalog Number | ASB-DG |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
Customer Support Contacts
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854648520 [Direct Marking] |
| GS1 | 10845854902073 [Previous] |
| GS1 | 30845854648524 [Primary] |
FDA Product Code
| HTW | BIT, DRILL |
| LXH | Orthopedic manual surgical instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
[30845854648524]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-03 |
| Device Publish Date | 2020-08-26 |
On-Brand Devices [MicroLink]
| 10845854901335 | MicroLink™ CMC Trapezium Pin |
| 20845854600013 | MicroLink™ CMC Trapezium Pin |
| 10845854902080 | MicroLink™ CMC Drill Guide with Paddle |
| 10845854902073 | MicroLink™ CMC Drill Guide |
| 30845854648531 | MICROLINK, CMC DRILL GUIDE WITH PADDLE |
| 30845854648524 | MICROLINK, CMC DRILL GUIDE |
| 30845854648906 | MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOPAQUE) |
| 30845854648890 | MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOPAQUE) |
| 30845854648883 | MICROLINK, CMC PASSING DRILL |
| 30845854648876 | MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOLUCENT) |
| 30845854648869 | MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOLUCENT) |
| 10845854901823 | MicroLink™ McGlamry Elevator |
| 30845854049017 | MicroLink™ McGlamry Elevator |
| 40845854648903 | MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOPAQUE) |
| 40845854648897 | MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOPAQUE) |
| 40845854648873 | MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOLUCENT) |
| 40845854648866 | MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOLUCENT) |
Trademark Results [MicroLink]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MICROLINK 97750645 not registered Live/Pending |
COG Marketers. Ltd. 2023-01-11 |
 MICROLINK 97501151 not registered Live/Pending |
LifeNet Health 2022-07-13 |
 MICROLINK 97394950 not registered Live/Pending |
Nite Ize, Inc. 2022-05-04 |
 MICROLINK 88791935 not registered Live/Pending |
Troll Systems Corporation 2020-02-10 |
 MICROLINK 87680041 not registered Live/Pending |
LifeNet Health 2017-11-10 |
 MICROLINK 77293970 3667270 Live/Registered |
CHENG UEI PRECISION INDUSTRY CO. LTD. 2007-10-02 |
 MICROLINK 77046755 3825443 Live/Registered |
Centipede Systems, Inc. 2006-11-17 |
 MICROLINK 76574008 2922464 Dead/Cancelled |
SONOVA HOLDING AG 2004-01-23 |
 MICROLINK 75394531 not registered Dead/Abandoned |
AudioPack Sound Systems, Inc. 1997-11-21 |
 MICROLINK 74565430 2104514 Dead/Cancelled |
ELSA GMBH 1994-08-25 |
 MICROLINK 73793709 1572050 Dead/Cancelled |
JACOBSON, THERESA E. 1989-04-17 |
 MICROLINK 73639029 1520102 Dead/Cancelled |
CHEMICAL NEW YORK CORPORATION 1987-01-09 |
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