FDA UDI In Commercial Distribution 🇺🇸 United States

AMDS Hybrid Prosthesis ("AMDS")

DI: 00877234001192 · Model: K039420 · Artivion, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AMDS Hybrid Prosthesis ("AMDS")
Primary DI
00877234001192
Version / Model
K039420
Catalog Number
AMDS40
Company Name
Artivion, Inc.
Labeler DUNS
119253177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-05
Public Version
1
Public Version Date
2025-02-13
Public Version Status
New
Public Device Record Key
097aa6d4-3029-4fc5-900d-8b9f5581d3b1

Device Description

40mm Straight Stent (24mm collar)

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QSK Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

GMDN Terms

Code Name
43521 Bare-metal aortic stent

Identifiers

Type ID
Primary 00877234001192

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
H230007 000

Device Sizes

Type Value Unit Text
Catheter Length 527 Millimeter
Device Size Text, specify Aortic Stent Proximal Diameter: 20-35mm
Device Size Text, specify Aortic Stent Distal Diameter: 25-35mm
Device Size Text, specify Aortic Stent Minimum Length:153mm
Device Size Text, specify Aortic Stent Maximum Length:207mm
Device Size Text, specify Stent Collar Diameter: 24mm

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 25 Degrees Celsius