CHARLOTTE
GUDID 00889797012263
WRIGHT MEDICAL TECHNOLOGY, INC.
Surgical drill guide, reusable| Primary Device ID | 00889797012263 |
| NIH Device Record Key | a77a995c-f8a9-4b24-86dc-b996b2b0fd63 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CHARLOTTE |
| Version Model Number | 43510126 |
| 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 |
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889797012263 [Primary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
[00889797012263]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2016-09-17 |
On-Brand Devices [CHARLOTTE]
Trademark Results [CHARLOTTE]
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