PINN-ACL CPS-8909
GUDID 20845854026875
9MM PINN-ACL CROSSPIN POSITIONING ROD
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| Primary Device ID | 20845854026875 |
| NIH Device Record Key | c444ade8-656d-415a-be25-11b9ef386480 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PINN-ACL |
| Version Model Number | CPS-8909 |
| Catalog Number | CPS-8909 |
| 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(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
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 |
| 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 |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854026878 [Primary] |
| GS1 | 20845854026875 [Direct Marking] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
[20845854026875]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-02 |
| Device Publish Date | 2020-09-24 |
On-Brand Devices [PINN-ACL]
| 20845854014179 | 9MM PINN-ACL CROSSPIN SYSTEM, GRAFT HARNESS WITH CANNULA |
| 20845854013806 | PINN-ACL CROSSPIN SYSTEM, 45MM (20MM) CROSSPIN |
| 20845854013653 | PINN-ACL CROSSPIN SYSTEM, 50MM (25MM) CROSSPIN |
| 20845854013646 | 8MM PINN-ACL CROSS PIN SYSTEM, GRAFT HARNESS WITH CANNULA |
| 20845854013639 | PINN-ACL CROSSPIN SYSTEM, 40MM (15MM) CROSSPIN |
| 20845854034689 | 8MM PINN-ACL CROSSPIN POSITIONING ROD |
| 20845854034672 | PINN-ACL CROSSPIN DRIVER |
| 20845854034665 | PINN-ACL CROSSPIN U-GUIDE |
| 20845854026875 | 9MM PINN-ACL CROSSPIN POSITIONING ROD |
| 20845854026868 | PINN-ACL CROSSPIN DRILL BIT |
| 20845854026851 | PINN-ACL CROSSPIN STERILIZATION TRAY |
| 20845854025519 | PINN-ACL CRUCIATE GUIDE |
Trademark Results [PINN-ACL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PINN-ACL 74293602 1840425 Live/Registered |
CONMED CORPORATION 1992-07-13 |
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