Duns Number:342582423
Device Description: PERIOTOM FIG.2
Catalog Number
L-72
Brand Name
BMT Medizintechnik GmbH
Version/Model Number
L-72
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"
Yes
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
-
Product Code
EJB
Product Code Name
HANDLE, INSTRUMENT, DENTAL
Public Device Record Key
cebc5c96-b5cb-495b-8641-a8c894f2fbaf
Public Version Date
December 04, 2020
Public Version Number
2
DI Record Publish Date
May 05, 2020
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 | 2079 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1 |