Duns Number:789127011
Device Description: P9552F - Grounding Pads, Corded, Adult, Foam, Dual Pad, Horizontal (1pc per pouch, 25pc p P9552F - Grounding Pads, Corded, Adult, Foam, Dual Pad, Horizontal (1pc per pouch, 25pc per box, 8box per case)
Catalog Number
-
Brand Name
Bio Protech
Version/Model Number
P9552F
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
K073360,K073360,K073360
Product Code
GEI
Product Code Name
Electrosurgical, Cutting & Coagulation & Accessories
Public Device Record Key
4101f9f5-c96e-4ffe-8f9f-af330d1ce9c5
Public Version Date
September 07, 2022
Public Version Number
5
DI Record Publish Date
June 06, 2017
Package DI Number
10817120020743
Quantity per Package
100
Contains DI Package
00817120020746
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Master Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 103 |