Duns Number:381582196
Device Description: Piezotome® 2 pack (without tip) Delivered with an autoclavable Piezotome® 2 handpiecewith Piezotome® 2 pack (without tip) Delivered with an autoclavable Piezotome® 2 handpiecewith cord and a Piezotome® dynamometric wrench
Catalog Number
F87523
Brand Name
ACTEON
Version/Model Number
PACK PIEZOTOME 2
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K091331
Product Code
DZI
Product Code Name
Drill, Bone, Powered
Public Device Record Key
d0b7b024-be42-4584-b873-8ad2ecb51423
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 8 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 416 |