FDA UDI In Commercial Distribution 🇺🇸 United States

Neptune E-SEP

DI: 07613327299885 · Model: 0703005165 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Neptune E-SEP
Primary DI
07613327299885
Version / Model
0703005165
Catalog Number
0703-005-165
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
2e595c01-c049-4c3b-815a-9cc44d615881

Device Description

Neptune E-SEP 165mm Suction Sleeve

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 37613327299886
Primary 07613327299885

Customer Contacts

Device Sizes

Type Value Unit Text
Length 165.0 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity