FDA UDI Not in Commercial Distribution 🇺🇸 United States

Contegra®

DI: 00613994600301 · Model: 200H18 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Contegra®
Primary DI
00613994600301
Version / Model
200H18
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
18007994-fca1-4b6b-957a-a9f8bf3bf086
Distribution End Date
2018-10-05

Device Description

CNDT 200H18 CONTEGRA UNSUPP HDE PS

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
MWH pulmonic valved conduit

GMDN Terms

Code Name
60337 Pulmonary heart valve bioprosthesis

Identifiers

Type ID
Primary 00613994600301

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
H020003 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Valve Size 18 MM

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius