Duns Number:249675476
Device Description: Manual Med/Surg articulated bed.
Catalog Number
FL23SM
Brand Name
Manual Bed
Version/Model Number
FL23SM
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 21, 2016
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FNJ
Product Code Name
Bed, Manual
Public Device Record Key
b9ed9525-6ecc-4c22-9052-7e5ba26e365d
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
November 30, 2016
Package DI Number
26704820000032
Quantity per Package
1
Contains DI Package
16704820000035
Package Discontinue Date
September 21, 2016
Package Status
Not 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 | 6 |
2 | A medical device with a moderate to high risk that requires special controls. | 32 |