FDA UDI In Commercial Distribution 🇺🇸 United States

Bovie

DI: 00607151018030 · Model: A803 · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bovie
Primary DI
00607151018030
Version / Model
A803
Catalog Number
A803
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b5cb3b5d-5cff-496a-b66d-2752a3f99116

Device Description

FOOT SWITCH

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 00607151018030