Duns Number:025460908
Device Description: DRAWER TWO #IMF 109694
Catalog Number
ACCVB1000
Brand Name
Medline Industries, Inc.
Version/Model Number
ACCVB1000
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
-
Product Code
LYV
Product Code Name
LABEL OR TAG, STERILE
Public Device Record Key
7d836a1a-36e7-4275-9293-412c20a54955
Public Version Date
June 17, 2022
Public Version Number
5
DI Record Publish Date
October 06, 2019
Package DI Number
40193489804660
Quantity per Package
6
Contains DI Package
10193489804669
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 |