FDA UDI In Commercial Distribution 🇺🇸 United States

Sonata® Dispersive Electrode

DI: 10817929020364 · Model: DE-001 · GYNESONICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Sonata® Dispersive Electrode
Primary DI
10817929020364
Version / Model
DE-001
Catalog Number
DE-001
Company Name
GYNESONICS, INC.
Labeler DUNS
618493741
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-07
Public Version
1
Public Version Date
2021-07-15
Public Version Status
New
Public Device Record Key
6e2e1fe0-3d7a-47f4-be55-5c43da836bcb

Device Description

Electrosurgical return electrode, single-use

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
No
Sterilization Prior Use
No

Product Codes

Code Name
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Package 30817929020368
Primary 10817929020364

Customer Contacts

Phone
650-216-3860

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius