Infinity KRR110
GUDID 20845854083557
Infinity Retro-Reamer 11mm
Conmed Corporation
Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use| Primary Device ID | 20845854083557 |
| NIH Device Record Key | 847f5af1-e128-4679-bf9e-4a9997998cce |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Infinity |
| Version Model Number | KRR110 |
| Catalog Number | KRR110 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
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| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854083557 [Primary] |
| GS1 | 20845854902032 [Previous] |
FDA Product Code
| GFG | BIT, SURGICAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20845854083557]
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Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-30 |
| Device Publish Date | 2021-08-21 |
On-Brand Devices [Infinity]
| 30845854902329 | Infinity Anteromedial Guide Right 9/10mm |
| 30845854902312 | Infinity Anteromedial Guide Right 7/8mm |
| 30845854902305 | Infinity Anteromedial Guide Left 9/10mm |
| 30845854902299 | Infinity Anteromedial Guide Left 7/8mm |
| 30845854902282 | Infinity Guide Body |
| 30845854902275 | Infinity 3.5mm All-Inside Guide Sleeve |
| 30845854902268 | Infinity 2.4mm Guide Sleeve Angled |
| 30845854902251 | Infinity 2.4mm Guide Sleeve Straight |
| 30845854902244 | Infinity PCL Tibial Guide |
| 30845854902237 | Infinity ACL Tibial Tip Guide |
| 30845854902220 | Infinity ACL Tibial Elbow Guide |
| 30845854902213 | Infinity ACL Tibial Footprint Guide |
| 30845854902206 | Infinity ACL/PCL Femoral Footprint Guide |
| 30845854902190 | Infinity 3.5mm Tunnel Dilator |
| 30845854901674 | KPS Infinity Insert Tray |
| 30845854902060 | Infinity Suture Shuttle |
| 20845854902049 | Infinity Retro-Reamer 12mm |
| 20845854902032 | Infinity Retro-Reamer 11mm |
| 20845854902025 | Infinity Retro-Reamer 10mm |
| 20845854902018 | Infinity Retro-Reamer 9.5mm |
| 20845854902001 | Infinity Retro-Reamer 9mm |
| 20845854901998 | Infinity Retro-Reamer 8.5mm |
| 20845854901981 | Infinity Retro-Reamer 8mm |
| 20845854901974 | Infinity Retro-Reamer 7.5mm |
| 20845854901967 | Infinity Retro-Reamer 7mm |
| 20845854901950 | Infinity Retro-Reamer 6.5mm |
| 20845854901943 | Infinity Retro-Reamer 6mm |
| 30845854901810 | Infinity™ 3.5mm Spade Tip Guide Pin |
| 30845854648814 | Infinity PCL Tibial Guide |
| 30845854648784 | Infinity Guide Body |
| 30845854648777 | Infinity ACL/PCL Femoral Footprint Guide |
| 30845854648760 | Infinity Anteromedial Guide Right 9/10mm |
| 20845854901806 | Infinity™ Adjustable Free Loop |
| 20845854901790 | Infinity™ Femoral Adjustable Loop Button |
| 10845854901786 | Infinity™ Adjustable Loop Button Cradle |
| 10845854901779 | Infinity™ Large Tibial Button |
| 10845854901762 | Infinity™ Standard Tibial Button |
| 20845854648978 | Infinity™ 3.5mm Spade Tip Guide Pin |
| 20845854649111 | Infinity™ Large Tibial Button |
| 20845854649104 | Infinity™ Standard Tibial Button |
| 20845854649074 | Infinity™ Adjustable Loop Button Cradle |
| 20845854649067 | Infinity™ Femoral Adjustable Loop Button |
| 30845854083639 | Infinity 3.5mm Tunnel Dilator |
| 30845854083578 | Infinity Suture Shuttle |
| 20845854083564 | Infinity Retro-Reamer 12mm |
| 20845854083557 | Infinity Retro-Reamer 11mm |
| 20845854083540 | Infinity Retro-Reamer 10mm |
| 20845854083472 | Infinity Retro-Reamer 6.5mm |
| 20845854083465 | Infinity Retro-Reamer 6mm |
| 10845854648841 | Infinity 2.4mm Guide Sleeve Angled |
Trademark Results [Infinity]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INFINITY 98470220 not registered Live/Pending |
IBF IP, LLC 2024-03-27 |
 INFINITY 98466286 not registered Live/Pending |
IBF IP, LLC 2024-03-25 |
 INFINITY 98454204 not registered Live/Pending |
Tanks By Mail Inc 2024-03-18 |
 INFINITY 98433629 not registered Live/Pending |
Infinity Generation Inc. 2024-03-05 |
 INFINITY 98338571 not registered Live/Pending |
Careismatic Brands, LLC 2024-01-02 |
 INFINITY 98293120 not registered Live/Pending |
PREFERRED COLLECTIONS INC. 2023-11-30 |
 INFINITY 98275942 not registered Live/Pending |
Capital One Financial Corporation 2023-11-17 |
 INFINITY 98242984 not registered Live/Pending |
IGH Holding Inc. 2023-10-27 |
 INFINITY 98175956 not registered Live/Pending |
CellFE, Inc. 2023-09-12 |
 INFINITY 98171540 not registered Live/Pending |
AccuTec, Inc. 2023-09-08 |
 INFINITY 98058654 not registered Live/Pending |
Encore RV LLC 2023-06-26 |
 INFINITY 98049650 not registered Live/Pending |
Induplate Operations, LLC 2023-06-19 |
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