VerteFIT VF9117R
GUDID 03662663033282
LDR Spine Usa, Inc.
Orthopaedic implant inserter/extractor, reusable| Primary Device ID | 03662663033282 |
| NIH Device Record Key | c718657c-c073-4278-bdf6-ad632cb46388 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VerteFIT |
| Version Model Number | VF9117R |
| Catalog Number | VF9117R |
| Company DUNS | 615789729 |
| Company Name | LDR Spine Usa, 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 | 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 | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com |
Device Dimensions
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
| Length | 100 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03662663033282 [Primary] |
FDA Product Code
| LXH | Orthopedic Manual Surgical Instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
[03662663033282]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2018-12-12 |
On-Brand Devices [VerteFIT]
| 03662663033282 | VF9117R |
| 03662663033275 | VF9116R |
| 03662663033114 | VF9012R |
| 03662663036184 | VF3102T |
| 03662663036177 | VF2102T |
| 03662663036160 | VF1102T |
| 03662663049290 | VF991C-CR |
| 03662663049283 | VF991B-CR |
| 03662663049276 | VF991A-CR |
| 03662663049238 | VF990-CR |
| 03662663036153 | VF9192R |
| 03662663036146 | VF9191R |
| 03662663036139 | VF9190R |
| 03662663035422 | VF9118R |
| 03662663035170 | VF9013R |
| 03662663033268 | VF9115R |
| 03662663033213 | VF9110R |
| 03662663033206 | VF9109R |
| 03662663033190 | VF9108R |
| 03662663033183 | VF9107R |
| 03662663033107 | VF9011R |
| 03662663033077 | VF9008R |
| 03662663033060 | VF9007R |
| 03662663033053 | VerteFIT |
Trademark Results [VerteFIT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VERTEFIT 86539376 not registered Dead/Abandoned |
LDR Medical, S.A.S. 2015-02-19 |
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