FDA UDI In Commercial Distribution 🇺🇸 United States

Hancock™ II 7505

DI: 00763000614034 · Model: 7505SET · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Hancock™ II 7505
Primary DI
00763000614034
Version / Model
7505SET
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-03
Public Version
1
Public Version Date
2025-03-11
Public Version Status
New
Public Device Record Key
a4d4b80c-e7c8-446c-bf90-28a8e47b5efa

Device Description

OBTURATOR 7505SET HK II AORTIC MDR

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 00763000614034

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Content: 21, 23, 25, 27, 29 mm