Duns Number:713565195
Device Description: Adjust the depth that the needle is inserted. The slide stopper differs for each needle. U Adjust the depth that the needle is inserted. The slide stopper differs for each needle. Use a slide stopper that suits each type of needle being used.
Catalog Number
-
Brand Name
Slide stopper TEST
Version/Model Number
LATERAL NEEDLE STOPPER TEST E
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"
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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
MUE
Product Code Name
Full field digital,system,x-ray,mammographic
Public Device Record Key
ce0e088e-a922-454d-bab5-8beb10b8c9d5
Public Version Date
April 27, 2021
Public Version Number
3
DI Record Publish Date
September 16, 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 | 43 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 324 |
| 3 | A medical device with high risk that requires premarket approval | 1 |