ULTRAFIX 10025
GUDID 20845854037024
ULTRAFIX DRILL 3.2MM
Conmed Corporation
Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable| Primary Device ID | 20845854037024 |
| NIH Device Record Key | f5ffdc18-c150-415e-a9ca-946a59cda3d9 |
| Commercial Distribution Discontinuation | 2024-02-21 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ULTRAFIX |
| Version Model Number | 10025 |
| Catalog Number | 10025 |
| 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
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com |
Device Dimensions
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
| Outer Diameter | 3.2 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854037027 [Primary] |
| GS1 | 20845854037024 [Direct Marking] |
FDA Product Code
| GFG | BIT, SURGICAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
[20845854037024]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-02-22 |
| Device Publish Date | 2020-09-24 |
On-Brand Devices [ULTRAFIX]
| 30845854037144 | ULTRAFIX MICROMITE DRILL, 1.8MM |
| 30845854037113 | ULTRAFIX ARTHROSCOPIC DRILL, 2.4MM |
| 30845854037106 | ULTRAFIX DRILL, 2.4MM |
| 30845854037076 | ULTRAFIX ARTHROSCOPIC DRILL GUIDE |
| 30845854037021 | ULTRAFIX DRILL 3.2MM |
| 30845854037014 | ULTRAFIX DRILL GUIDE |
| 30845854024199 | ULTRAFIX ARTHROSCOPIC INSERTER |
| 20845854024192 | ULTRAFIX ARTHROSCOPIC INSERTER |
| 20845854037062 | ULTRAFIX ARTHROSCOPIC DRILL, 3.2MM |
| 20845854037024 | ULTRAFIX DRILL 3.2MM |
Trademark Results [ULTRAFIX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ULTRAFIX 98525541 not registered Live/Pending |
9485-7489 Quebec Inc. 2024-04-29 |
 ULTRAFIX 78031285 2494514 Dead/Cancelled |
Green, Tommy Joe O. 2000-10-18 |
 ULTRAFIX 75003610 2162402 Live/Registered |
CONMED CORPORATION 1995-10-03 |
 ULTRAFIX 74380431 1887717 Live/Registered |
EK Industries, Inc. 1993-04-15 |
 ULTRAFIX 72051855 0702059 Dead/Cancelled |
Brown-Forman Distillers Corporation 1958-05-19 |
 ULTRAFIX 71666887 0600232 Dead/Expired |
VERONA CHEMICAL COMPANY 1954-05-21 |
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