FDA UDI In Commercial Distribution 🇺🇸 United States

MECTRON

DI: E322031202490010 · Model: MANIPOLO PIEZOSURGERY® medical + · MECTRON SPA
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MECTRON
Primary DI
E322031202490010
Version / Model
MANIPOLO PIEZOSURGERY® medical +
Catalog Number
03120249-001
Company Name
MECTRON SPA
Labeler DUNS
436664734
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-16
Public Version
1
Public Version Date
2025-06-24
Public Version Status
New
Public Device Record Key
a30a19e4-b31d-4551-beb1-63b68720ad1f

Device Description

Ultrasonic Medical Handpiece

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
Yes
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
DZI Drill, Bone, Powered
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
JDX Instrument, Surgical, Sonic And Accessory/Attachment

GMDN Terms

Code Name
47014 Dental ultrasonic surgical system handpiece

Identifiers

Type ID
Primary E322031202490010

Customer Contacts

Phone
+16144594922

Premarket Submissions

Submission Number Supplement Number
K153743 000