FDA UDI In Commercial Distribution 🇺🇸 United States

Bovie

DI: 10607151005884 · Model: IDS-300-REBURBISHED · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bovie
Primary DI
10607151005884
Version / Model
IDS-300-REBURBISHED
Catalog Number
IDS-300-REBURBISHED
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-13
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
332d4aea-0fc4-45e6-914d-41dc09c03f0d

Device Description

BOVIE IDS-300-REFURBISHED HIGH FREQUENCY ELECTROSURGICAL GENERATOR

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 10607151005884

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity