Duns Number:961027315
Device Description: Surgical Gown, LG
Catalog Number
9010
Brand Name
CONVERTORS
Version/Model Number
9010
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 19, 2022
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
Yes
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
FYA
Product Code Name
GOWN, SURGICAL
Public Device Record Key
3a9e1830-dbca-4801-a32f-ab4b5f0cedde
Public Version Date
June 21, 2022
Public Version Number
7
DI Record Publish Date
October 31, 2018
Package DI Number
50885380156456
Quantity per Package
20
Contains DI Package
10885380156458
Package Discontinue Date
June 19, 2022
Package Status
Not in Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |