FDA UDI In Commercial Distribution 🇺🇸 United States

ACTEON

DI: 03609820875231 · Model: PACK PIEZOTOME 2 · SATELEC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACTEON
Primary DI
03609820875231
Version / Model
PACK PIEZOTOME 2
Catalog Number
F87523
Company Name
SATELEC
Labeler DUNS
381582196
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d0b7b024-be42-4584-b873-8ad2ecb51423

Device Description

Piezotome® 2 pack (without tip) Delivered with an autoclavable Piezotome® 2 handpiece with cord and a Piezotome® dynamometric wrench

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

GMDN Terms

Code Name
47014 Dental ultrasonic surgical system handpiece

Identifiers

Type ID
Primary 03609820875231

Customer Contacts

Phone
+33556340607

Premarket Submissions

Submission Number Supplement Number
K091331 000