FDA UDI In Commercial Distribution 🇺🇸 United States

SimuPlus™

DI: 00763000659332 · Model: 7700FB34 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SimuPlus™
Primary DI
00763000659332
Version / Model
7700FB34
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-02
Public Version
1
Public Version Date
2026-02-10
Public Version Status
New
Public Device Record Key
31a7ef3c-9fa4-4231-8c40-a058fa34506c

Device Description

BAND 7700FB34 SIMUPLUS FLEX 34MM MDR

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRH RING, ANNULOPLASTY

GMDN Terms

Code Name
66338 Mitral/tricuspid annuloplasty ring, open-surgery

Identifiers

Type ID
Primary 00763000659332

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201449 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 34.0 Millimeter