FDA UDI In Commercial Distribution 🇺🇸 United States

Neptune E-SEP

DI: 07613327297973 · Model: 0703-120-003 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Neptune E-SEP
Primary DI
07613327297973
Version / Model
0703-120-003
Catalog Number
0703-120-003
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2021-02-22
Public Version Status
Update
Public Device Record Key
4c61574f-abdf-44b3-ae62-da4001bffe79

Device Description

Neptune E-SEP 3mm Ball Electrode

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
61869 Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Package 37613327297974
Primary 07613327297973

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 3.0 Millimeter