FDA UDI In Commercial Distribution 🇺🇸 United States

DYONICS / ELECTROBLADE

DI: 03596010466150 · Model: 7205961 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DYONICS / ELECTROBLADE
Primary DI
03596010466150
Version / Model
7205961
Catalog Number
7205961
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-23
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
35ef52b1-5bff-4f71-a5fe-4d033264102d

Device Description

ELECTROBLADE RESECTOR 4.5MM (3)

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
56296 Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Package 23596010466154
Primary 03596010466150

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K012314 000