FDA UDI Not in Commercial Distribution 🇺🇸 United States

TRIVEX

DI: 03596010460172 · Model: 7205942 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRIVEX
Primary DI
03596010460172
Version / Model
7205942
Catalog Number
7205942
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-23
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
3a71952d-c525-4216-b863-b7acd0775aa2
Distribution End Date
2016-09-21

Device Description

MTO TRIVEX TM GERMAN KIT 230-240V

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
42365 Transillumination phlebectomy system control unit

Identifiers

Type ID
Primary 03596010460172

Customer Contacts