Duns Number:314546664
Device Description: BodyFIX® Hygienic Drape Manifold Tube (2x15000mm) is used to cover the manifold tube for h BodyFIX® Hygienic Drape Manifold Tube (2x15000mm) is used to cover the manifold tube for hygienic purposes.
Catalog Number
P10102-305
Brand Name
BodyFIX
Version/Model Number
P10102-305
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
-
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
K121530,K121530
Product Code
IYE
Product Code Name
Accelerator, Linear, Medical
Public Device Record Key
f77fa640-8aa0-4cf1-aa3a-546da1bb170c
Public Version Date
October 12, 2021
Public Version Number
3
DI Record Publish Date
August 23, 2016
Package DI Number
04056719000264
Quantity per Package
5
Contains DI Package
04056719001728
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 175 |