FDA UDI In Commercial Distribution 🇺🇸 United States

Neptune E-SEP

DI: 07613327297942 · Model: 0703-213-020 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Neptune E-SEP
Primary DI
07613327297942
Version / Model
0703-213-020
Catalog Number
0703-213-020
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
5690f404-b9ec-4823-a2e6-c51d20281e08

Device Description

Neptune E-SEP Conization Electrode W13 D20 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 37613327297943
Primary 07613327297942

Customer Contacts

Device Sizes

Type Value Unit Text
Depth 20.0 Millimeter
Length 120.0 Millimeter
Width 13.0 Millimeter