Simulus™
GUDID 00763000318536
HANDLE 752 SIMULUS ANNULOPLASTY CE
MEDTRONIC 3F THERAPEUTICS, INC.
Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable Heart valve annulus sizer, reusable| Primary Device ID | 00763000318536 |
| NIH Device Record Key | 1000af4d-fdb1-4a52-8040-7e13e9f265d1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Simulus™ |
| Version Model Number | 752 |
| Company DUNS | 079527232 |
| Company Name | MEDTRONIC 3F THERAPEUTICS, 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 | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000318536 [Primary] |
FDA Product Code
| DTI | SIZER, HEART-VALVE, PROSTHESIS |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
[00763000318536]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-14 |
| Device Publish Date | 2021-06-06 |
On-Brand Devices [Simulus™]
| 00763000318543 | SIZER SET 850 SEMI-RIDGID SIMULUS CE |
| 00763000318536 | HANDLE 752 SIMULUS ANNULOPLASTY CE |
| 00763000318512 | SIZER SET 750 SIMULUS FLEXIBLE 1L CE |
| 00763000318529 | SIZER SET 755 SIMULUS FLEXIBLEROBOTIC CE |
Trademark Results [Simulus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SIMULUS 79085926 4103578 Dead/Cancelled |
Agence Spatiale Européenne (ESA) 2010-06-16 |
 SIMULUS 78735472 3287012 Live/Registered |
MEDTRONIC ATS MEDICAL, INC. 2005-10-18 |
 SIMULUS 75530586 2369328 Dead/Cancelled |
Simulus, Ltd. 1998-08-04 |
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