FDA UDI In Commercial Distribution 🇺🇸 United States

Simulus™

DI: 00643169707535 · Model: 750 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Simulus™
Primary DI
00643169707535
Version / Model
750
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-30
Public Version
1
Public Version Date
2025-06-09
Public Version Status
New
Public Device Record Key
0ba6d774-f05a-4ead-ad77-8be426b4707a

Device Description

ACCY KIT 750 SIMULUS FLEXIBLE RING/BAN

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
DTI SIZER, HEART-VALVE, PROSTHESIS

GMDN Terms

Code Name
47684 Heart valve annulus sizer, reusable

Identifiers

Type ID
Primary 00643169707535

Customer Contacts