METRx® System
GUDID 00885074210353
ENDOSCOPE 9560100 MED REUSABLE
MEDTRONIC SOFAMOR DANEK, INC.
Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable| Primary Device ID | 00885074210353 |
| NIH Device Record Key | 238fd937-3f75-4f3d-ad79-ed90fabb0cbe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | METRx® System |
| Version Model Number | 9560100 |
| Company DUNS | 830350380 |
| Company Name | MEDTRONIC SOFAMOR DANEK, INC. |
| 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 | 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)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00885074210353 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K002931
FDA Product Code
| HRX | Arthroscope |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
[00885074210353]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-15 |
| Device Publish Date | 2019-03-07 |
On-Brand Devices [METRx® System]
| 00613994415868 | RETRACTOR X1007055 MX TUBE 26MM X 10CM |
| 00613994393623 | RETRACTOR X0907067 25MM X 9CM EXPANDING |
| 00613994312129 | TUBE 9565670 16MMX3CM COATED |
| 00613994312112 | TUBE 9565671 16MMX4CM COATED |
| 00613994312105 | TUBE 9565672 16MMX5CM COATED |
| 00613994312099 | TUBE 9565673 16MMX6CM COATED |
| 00613994312082 | TUBE 9565674 16MMX7CM COATED |
| 00613994312075 | TUBE 9565675 16MMX8CM COATED |
| 00613994312068 | TUBE 9565676 16MMX9CM COATED |
| 00613994312051 | TUBE 9565666 14MMX9CM COATED |
| 00613994312044 | TUBE 9565665 14MMX8CM COATED |
| 00613994312037 | TUBE 9565664 14MMX7CM COATED |
| 00613994312020 | TUBE 9565663 14MMX6CM COATED |
| 00613994312013 | TUBE 9565662 14MMX5CM COATED |
| 00613994312006 | TUBE 9565661 14MMX4CM COATED |
| 00613994311993 | TUBE 9565660 14MMX3CM COATED |
| 00613994311986 | TUBE 9565726 20MMX9CM COATED |
| 00613994311979 | TUBE 9565725 20MMX8CM COATED |
| 00613994311962 | TUBE 9565724 20MMX7CM COATED |
| 00613994311955 | TUBE 9565723 20MMX6CM COATED |
| 00613994311948 | TUBE 9565722 20MMX5CM COATED |
| 00613994311931 | TUBE 9565721 20MMX4CM COATED |
| 00613994311924 | TUBE 9565720 20MMX3CM COATED |
| 00613994311900 | TUBE 9565685 18MMX8CM COATED |
| 00613994311894 | TUBE 9565684 18MMX7CM COATED |
| 00613994311887 | TUBE 9565683 18MMX6CM COATED |
| 00613994311870 | TUBE 9565682 18MMX5CM COATED |
| 00613994311863 | TUBE 9565681 18MMX4CM COATED |
| 00613994311856 | TUBE 9565680 18MMX3CM COATED |
| 00613994286291 | RETRACTOR X1106107 18MM X 9CM TUBE |
| 00673978961170 | CASE 9560698 METRX MD BASE CASE |
| 00673978085609 | INSTRUMENT 9560180 18MM MTRXND ATCH STRL |
| 00673978085593 | INSTRUMENT 9560160 16MM MTRXND ATCH STRL |
| 00673978085524 | INSTRUMENT 9560107 3 CHIP CAM ADPTR |
| 00673978085487 | SCOPE 9560102 MTRX REUSE ENDOSCOPE LONG |
| 00721902949180 | 18MM RADIANCE ILLUM. SYSTEM |
| 00721902663444 | INSTRUMENT 9560757 RDINCEXILLUMIN SYS |
| 00721902444104 | INSTRUMENT 9560702 RADIANCE ILLUMIN SYS |
| 00885074458861 | TUBE 9569756 26MM X 9CM COATED |
| 00885074458847 | TUBE 9569755 26MM X 8CM COATED |
| 00885074458830 | TUBE 9569754 26MM X 7CM COATED |
| 00885074458816 | TUBE 9569753 COATED 26MM X 6CM |
| 00885074458809 | TUBE 9569752 COATED 26MMX5CM |
| 00885074458786 | TUBE 9569751 COATED 26MM X 4CM |
| 00885074458779 | TUBE 9569750 COATED 26MM X 3CM |
| 00885074458724 | TUBE 9569736 22MM X 9CM COATED |
| 00885074458700 | TUBE 9569735 22MM X 8CM COATED |
| 00885074458694 | TUBE 9569734 22MM X 7CM COATED |
| 00885074458663 | TUBE 9569733 22MM X 6CM COATED |
| 00885074458649 | TUBE 9569732 22MM X 5CM COATED |
Trademark Results [METRx]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 METRX 75777453 not registered Dead/Abandoned |
inQuire Group 1999-08-17 |
 METRX 75649462 3083108 Live/Registered |
WARSAW ORTHOPEDIC, INC. 1999-07-29 |
 METRX 73098289 1090019 Dead/Expired |
MOTOROLA, INC. 1976-08-30 |
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