Duns Number:025460908
Device Description: DBD-SEE MLABTP3SMBLB-PIPETTE,TRANS,3
Catalog Number
MLAB137035
Brand Name
Medline
Version/Model Number
MLAB137035
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GJW
Product Code Name
PIPETTE, PASTEUR
Public Device Record Key
053ba31b-9afe-478a-8bf6-65847ee85f7f
Public Version Date
November 10, 2021
Public Version Number
1
DI Record Publish Date
November 02, 2021
Package DI Number
40884389106991
Quantity per Package
10
Contains DI Package
30884389106994
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 | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |