FDA UDI In Commercial Distribution 🇺🇸 United States

Piezomed Pro Accessory

DI: J021305030231 · Model: 30503023 · W & H Dentalwerk Bürmoos GmbH
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Piezomed Pro Accessory
Primary DI
J021305030231
Version / Model
30503023
Company Name
W & H Dentalwerk Bürmoos GmbH
Labeler DUNS
300238441
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-22
Public Version
1
Public Version Date
2025-09-30
Public Version Status
New
Public Device Record Key
fa77a6c8-aac6-4e15-955a-868b83399f44

Device Description

Instrument MS12-S

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
DZI Drill, Bone, Powered
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
JDX Instrument, Surgical, Sonic And Accessory/Attachment

GMDN Terms

Code Name
45981 Hard/soft-tissue ultrasonic surgical system

Identifiers

Type ID
Primary J021305030231