FDA UDI In Commercial Distribution 🇺🇸 United States

Neptune E-SEP

DI: 07613327297959 · Model: 0703-315-012 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Neptune E-SEP
Primary DI
07613327297959
Version / Model
0703-315-012
Catalog Number
0703-315-012
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
6
Public Version Date
2021-02-22
Public Version Status
Update
Public Device Record Key
3f759c83-6e59-4844-a594-6973d8b1cf8a

Device Description

Neptune E-SEP Loop T-Bar Electrode W15 D12 L120

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 37613327297950
Primary 07613327297959

Customer Contacts

Device Sizes

Type Value Unit Text
Width 15.0 Millimeter
Length 120.0 Millimeter
Depth 12.0 Millimeter