Trocar ODI-T106
GUDID B058ODIT1061
Trocar
Orthopedic Designs North America, Inc.
Orthopaedic trocar blade, reusable| Primary Device ID | B058ODIT1061 |
| NIH Device Record Key | 8aecbe90-aec6-4c37-961e-609ffecb87b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trocar |
| Version Model Number | ODIT106 |
| Catalog Number | ODI-T106 |
| Company DUNS | 945518848 |
| Company Name | Orthopedic Designs North America, 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 | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com | |
| Phone | 888-635-8535 |
| support@odi-na.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B058ODIT1061 [Primary] |
FDA Product Code
| LXH | Orthopedic Manual Surgical Instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
[B058ODIT1061]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-21 |
| Device Publish Date | 2023-08-11 |
On-Brand Devices [Trocar]
| B058ODIT1061 | Trocar |
| B058ODIF151 | Trocar |
Trademark Results [Trocar]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TROCAR 86526529 4812059 Live/Registered |
FERADYNE OUTDOORS, LLC 2015-02-06 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.