FDA UDI In Commercial Distribution 🇺🇸 United States

Vein Distention

DI: 00803622133138 · Model: 400 · LIVANOVA USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vein Distention
Primary DI
00803622133138
Version / Model
400
Company Name
LIVANOVA USA, INC.
Labeler DUNS
080914995
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-09
Public Version
3
Public Version Date
2018-08-15
Public Version Status
Update
Public Device Record Key
6370e32e-ae69-44bb-bde9-b9fbe72777fa

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DWP DILATOR, VESSEL, SURGICAL

GMDN Terms

Code Name
11268 Vascular dilator, reusable

Identifiers

Type ID
Package 10803622133135
Primary 00803622133138