FDA UDI Not in Commercial Distribution 🇺🇸 United States

VP1200K™

DI: 05037881020051 · Model: 251010 · VASCUTEK LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VP1200K™
Primary DI
05037881020051
Version / Model
251010
Catalog Number
251010
Company Name
VASCUTEK LTD
Labeler DUNS
229053087
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-19
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
8b28f7d7-82e6-441a-b242-d0c28e9c727f
Distribution End Date
2018-11-20

Device Description

VP1200KAX-BIFEM RIGHT

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DSY PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER

GMDN Terms

Code Name
35281 Synthetic vascular graft

Identifiers

Type ID
Primary 05037881020051

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K034010 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 10 Millimeter
Length 100 Centimeter
Device Size Text, specify Branch length 60cm
Device Size Text, specify Branch diameter 10 mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a clean dry area
Type
Handling Environment Temperature
Temperature Range
0 – 50 Degrees Celsius