Duns Number:117174678
Device Description: Anesthesia Bundle
Catalog Number
-
Brand Name
Regard
Version/Model Number
AN01084D
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
OGD
Product Code Name
Custom Anesthesia Tray
Public Device Record Key
f4f83c59-2452-43a9-b3b2-0a48ef6feaa2
Public Version Date
August 31, 2021
Public Version Number
2
DI Record Publish Date
December 10, 2020
Package DI Number
20194717108921
Quantity per Package
15
Contains DI Package
10194717108924
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 589 |
2 | A medical device with a moderate to high risk that requires special controls. | 961 |