Duns Number:800450475
Device Description: I-BEAM AIR MATTRESS FOR FOAM T
Catalog Number
-
Brand Name
Meridian Medical
Version/Model Number
3102M
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FNM
Product Code Name
Mattress, Air Flotation, Alternating Pressure
Public Device Record Key
059f2da7-b7e2-4c90-a01d-9b5449288d1c
Public Version Date
July 09, 2018
Public Version Number
3
DI Record Publish Date
October 18, 2016
Package DI Number
30815067042594
Quantity per Package
2
Contains DI Package
00815067042593
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CA
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 6 |
2 | A medical device with a moderate to high risk that requires special controls. | 27 |