Duns Number:080030042
Device Description: PHB, Autoalert, Japan - Primary
Catalog Number
FD100-J
Brand Name
PHB, Autoalert, Japan - Primary
Version/Model Number
1840501
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 30, 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"
Yes
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
ILQ
Product Code Name
System, communication, powered
Public Device Record Key
6b7be79b-1af4-46b2-9349-60d75e686f37
Public Version Date
October 19, 2021
Public Version Number
3
DI Record Publish Date
June 30, 2016
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 92 |