FDA UDI In Commercial Distribution 🇺🇸 United States

HANCOCK II ULTRA®

DI: 00643169594616 · Model: T505U229 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HANCOCK II ULTRA®
Primary DI
00643169594616
Version / Model
T505U229
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-07
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
c8831558-978b-4ac9-84a8-6b7823530b0b

Device Description

VLV T505U229 HKII AORULT CII NNA US PEEK

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 Conditional
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
DYE replacement Heart-valve

GMDN Terms

Code Name
60242 Aortic heart valve bioprosthesis

Identifiers

Type ID
Primary 00643169594616

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P980043 048

Device Sizes

Type Value Unit Text
Device Size Text, specify Valve Size 29 MM

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 25 Degrees Celsius