Duns Number:134139174
Device Description: HemoSphere Roll Stand
Catalog Number
HEMRLSTD1000
Brand Name
HemoSphere
Version/Model Number
HEMRLSTD1000
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K163381
Product Code
DQE
Product Code Name
Catheter, Oximeter, Fiberoptic
Public Device Record Key
ff42f82e-ad61-48d1-b9b2-149c90b1228e
Public Version Date
August 09, 2021
Public Version Number
5
DI Record Publish Date
July 24, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 5 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 643 |
| 3 | A medical device with high risk that requires premarket approval | 212 |