Duns Number:801895244
Device Description: 17G Wallace Dual Lumen Oocyte Recovery Set, 950 mm tubing (Box of 10)
Catalog Number
-
Brand Name
17G Wallace Dual Lumen Oocyte Recovery Set
Version/Model Number
DNS1733-950
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
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
-
Product Code
MQE
Product Code Name
Needle, Assisted Reproduction
Public Device Record Key
cb246e20-054f-45cf-b7f7-904f25c78e7d
Public Version Date
December 12, 2019
Public Version Number
1
DI Record Publish Date
December 04, 2019
Package DI Number
30888937020947
Quantity per Package
10
Contains DI Package
20888937020940
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 29 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1471 |
| 3 | A medical device with high risk that requires premarket approval | 2 |