FDA UDI In Commercial Distribution 🇺🇸 United States

Neptune

DI: 07613327556544 · Model: 0703125201 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Neptune
Primary DI
07613327556544
Version / Model
0703125201
Catalog Number
0703-125-201
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-10
Public Version
1
Public Version Date
2024-12-18
Public Version Status
New
Public Device Record Key
67b4e995-20cc-43f2-a72f-a2e7bf833478

Device Description

SafeAir 125mm Blade Electrode, Non-Coated, Non-Sterile

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
Yes
Sterilization Methods
Ethylene Oxide

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 37613327556545
Primary 07613327556544

Customer Contacts

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