BIOARCH ST1020
GUDID 00889797053235
Probe Subtalar System
WRIGHT MEDICAL TECHNOLOGY, INC.
Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable 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 | 00889797053235 |
| NIH Device Record Key | a4b673ce-e831-4f35-a7f0-e2c2a6c7ea8f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOARCH |
| Version Model Number | ST1020 |
| Catalog Number | ST1020 |
| Company DUNS | 807201207 |
| Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
| 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)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889797053235 [Primary] |
FDA Product Code
| HXB | PROBE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
[00889797053235]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2022-08-11 |
| Device Publish Date | 2017-01-26 |
On-Brand Devices [BIOARCH]
| 00889797053242 | ST1030 |
| 00840420128928 | ST1112 |
| 00840420128911 | ST1111 |
| 00840420128904 | ST1110 |
| 00840420128898 | ST1109 |
| 00840420128881 | ST1108 |
| 00889797053228 | Insertion Driver Subtalar System |
| 00889797055482 | Subtalar Implant Alignment Rod |
| 00889797055475 | Alignment Rod |
| 00889797053235 | Probe Subtalar System |
| 00889797053297 | Trial Sizer |
| 00889797053280 | Trial Sizer |
| 00889797053273 | Trial Sizer |
| 00889797053266 | Trial Sizer |
| 00889797053259 | Trial Sizer |
Trademark Results [BIOARCH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BIOARCH 77210412 3474925 Live/Registered |
Koby Ventures, L.P. 2007-06-20 |
 BIOARCH 74456420 1854561 Dead/Cancelled |
J2B2, Inc. 1993-11-03 |
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