Duns Number:130789944
Device Description: RFID Single Use 1000 Micron Laser Fiber
Catalog Number
HLFD1000C
Brand Name
Dornier MedTech
Version/Model Number
1000 Micron Single Use
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
Yes
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
K121938,K121938
Product Code
GEX
Product Code Name
Powered Laser Surgical Instrument
Public Device Record Key
674cbc06-6ff5-4481-9511-56466f0e6109
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 27, 2016
Package DI Number
00810116020126
Quantity per Package
3
Contains DI Package
00810116020034
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 28 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 101 |