FDA UDI In Commercial Distribution 🇺🇸 United States

VECTRA®, VASCULAR ACCESS GRAFT

DI: 00813024011323 · Model: 10002-5040-001 · Thoratec Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VECTRA®, VASCULAR ACCESS GRAFT
Primary DI
00813024011323
Version / Model
10002-5040-001
Catalog Number
10002-5040-001
Company Name
Thoratec Corporation
Labeler DUNS
070156955
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-20
Public Version
8
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
548661df-da0b-4f6b-9131-2f4658d5c02c

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
Labeling does not contain MRI Safety Information
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
DYF Prosthesis, Vascular Graft, Of Less Then 6mm Diameter

GMDN Terms

Code Name
13586 Arteriovenous shunt

Identifiers

Type ID
Primary 00813024011323

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius