Duns Number:125850144
Device Description: 19 Bi-Bevel Hoe (3-2-28)
Catalog Number
R420
Brand Name
PDT, Inc.
Version/Model Number
R420 19 Bi-Bevel Hoe (3-2-28)
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
EMQ
Product Code Name
Hoe, Periodontic
Public Device Record Key
edc2aa29-ed45-4064-b1b3-ea4c2db8c422
Public Version Date
May 17, 2022
Public Version Number
2
DI Record Publish Date
April 30, 2021
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 | 248 |