FDA UDI In Commercial Distribution 🇺🇸 United States

MECTRON

DI: E322045700031010 · Model: W3 -US- · MECTRON SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MECTRON
Primary DI
E322045700031010
Version / Model
W3 -US-
Catalog Number
04570003-101
Company Name
MECTRON SPA
Labeler DUNS
436664734
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-03
Public Version
1
Public Version Date
2023-05-11
Public Version Status
New
Public Device Record Key
75dcb807-9867-4fa2-83ad-03db0a8dd867

Device Description

Insert W3 it's used for smoothing the osteotomy walls during the implant site preparation.

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ELC Scaler, Ultrasonic

GMDN Terms

Code Name
47015 Dental ultrasonic surgical system handpiece tip

Identifiers

Type ID
Primary E322045700031010

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151248 000