ENDURA C9032
GUDID 30845854020368
4.5MM ENDURA VORTEX, UNHOODED
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 Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable Orthopaedic bur, reusable| Primary Device ID | 30845854020368 |
| NIH Device Record Key | 4efec3de-efec-4fc7-9007-e7d37ba48638 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENDURA |
| Version Model Number | C9032 |
| Catalog Number | C9032 |
| 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 | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 Millimeter |
| Outer Diameter | 4.5 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 |
| 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 | 20845854020361 [Primary] |
| GS1 | 30845854020368 [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 |
[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
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[30845854020368]
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[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
Radiation Sterilization
[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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[30845854020368]
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 [ENDURA]
| 30845854020405 | 5.5MM ENDURA FULL RADIUS RESECTOR |
| 30845854020399 | 4.2MM ENDURA FULL RADIUS RESECTOR |
| 30845854020382 | 3.5MM ENDURA FULL RADIUS RESECTOR |
| 30845854020368 | 4.5MM ENDURA VORTEX, UNHOODED |
| 30845854020351 | 4.5MM ENDURA VORTEX |
| 30845854020344 | 5.5MM ENDURA SPHERICAL BUR |
| 30845854020337 | 4.5 MM ENDURA SPHERICAL BUR |
| 30845854020320 | 3.5MM ENDURA SPHERICAL BUR |
Trademark Results [ENDURA]
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