Duns Number:604483321
Catalog Number
10220
Brand Name
BREG
Version/Model Number
PAD INTELLI FLO SHOULDER
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
ILO
Product Code Name
Pack, Hot Or Cold, Water Circulating
Public Device Record Key
826bbab9-0f9b-4bd1-b9e6-59f0d71db75d
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 15, 2016
Package DI Number
60672736001372
Quantity per Package
20
Contains DI Package
00672736001295
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Bulk 20 pack
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 129 |