FDA UDI In Commercial Distribution 🇺🇸 United States

Heli-FX™ EndoAnchor™ System

DI: 00763000006624 · Model: SG-64 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Heli-FX™ EndoAnchor™ System
Primary DI
00763000006624
Version / Model
SG-64
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-17
Public Version
7
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
368f0873-beac-4140-9bf7-b994981bfbbc

Device Description

AAA GUIDE DEVICE 22 EIFU

Device Characteristics

Single Use
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OTD Endovascular suturing system

GMDN Terms

Code Name
45612 Soft-tissue/mesh anchor, non-bioabsorbable

Identifiers

Type ID
Primary 00763000006624

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171427 000
K182957 000

Device Sizes

Type Value Unit Text
Length 62.0 Centimeter
Outer Diameter 5.3 Millimeter
Length 22.0 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry