FDA UDI In Commercial Distribution 🇺🇸 United States

WECK

DI: 00607151009786 · Model: 809317 · BOVIE MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
WECK
Primary DI
00607151009786
Version / Model
809317
Catalog Number
809317
Company Name
BOVIE MEDICAL CORPORATION
Labeler DUNS
079940465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-02
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
9889ab3e-913f-4779-8a25-3559824c83c8

Device Description

DISPOSABLE ¾” NEEDLE ELECTRODE 24/BX, 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
Yes
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
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
61874 Open-surgery electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Package 10607151009783
Primary 00607151009786