CUDA C9154
GUDID 30845854020412
4.2MM ENDURA CUDA
Conmed Corporation
Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable| Primary Device ID | 30845854020412 |
| NIH Device Record Key | 12446bf0-c9ba-4180-a9b8-1eec012ea32c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CUDA |
| Version Model Number | C9154 |
| Catalog Number | C9154 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | false |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
| Outer Diameter | 4.2 Millimeter |
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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854020415 [Primary] |
| GS1 | 30845854020412 [Direct Marking] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K943985
FDA Product Code
| HRX | ARTHROSCOPE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
[30845854020412]
Radiation Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [CUDA]
| 30845854020429 | 5.5MM ENDURA CUDA |
| 30845854020412 | 4.2MM ENDURA CUDA |
| 30845854013070 | 3.5MM ENDURA CUDA |
| 20845854029425 | 3.7MM, MERLIN 15 DEGREE CUDA, BENDABLE TO 30 DEGREE, 6 EA |
| 20845854020491 | 4.2MM, LARGE HUB, STERLING, SHAVER, CUDA |
| 20845854017538 | 4.2MM, LARGE HUB, STERLING, SHAVER, CUDA |
| 20845854017293 | 4.8MM, LARGE HUB, STERLING, SHAVER, CUDA |
| 20845854012571 | 2.9MM STERLING CUDA, 6 EA |
| 20845854010263 | CUDA, Bendable to 45 Degree |
Trademark Results [CUDA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CUDA 98526544 not registered Live/Pending |
FCA US LLC 2024-04-30 |
 CUDA 98423957 not registered Live/Pending |
NVIDIA Corporation 2024-02-27 |
 CUDA 97930280 not registered Live/Pending |
Buys, Jerry 2023-05-10 |
 CUDA 97923123 not registered Live/Pending |
Jerry Buys 2023-05-05 |
 CUDA 97592169 not registered Live/Pending |
Zvetco 2022-09-15 |
 CUDA 97515303 not registered Live/Pending |
Springhill Group, LLC 2022-07-22 |
 CUDA 90248316 not registered Live/Pending |
FCA US LLC 2020-10-12 |
 CUDA 88246397 not registered Live/Pending |
ACME UNITED CORPORATION 2019-01-01 |
 CUDA 87492424 not registered Live/Pending |
FCA US LLC 2017-06-16 |
 CUDA 87456192 not registered Dead/Abandoned |
CUDA Cooler Company, LLC 2017-05-18 |
 CUDA 87455883 not registered Dead/Abandoned |
CUDA Cooler Company, LLC 2017-05-18 |
 CUDA 87319037 not registered Live/Pending |
Cuda Pharmaceuticals, LLC 2017-01-31 |
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