Duns Number:961027315
Device Description: AMBITEX GLV EXAM NON-STERILE VINYL V200 CLEAR POWDER-FREE SMALL SMOOTH STANDARD LENGTH 10/ AMBITEX GLV EXAM NON-STERILE VINYL V200 CLEAR POWDER-FREE SMALL SMOOTH STANDARD LENGTH 10/100
Catalog Number
VSM200
Brand Name
AMBITEX
Version/Model Number
VSM200
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"
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
LYZ
Product Code Name
Vinyl patient examination glove
Public Device Record Key
ce4c3d4b-02c7-4490-ab2d-28c3d23b408e
Public Version Date
May 18, 2020
Public Version Number
2
DI Record Publish Date
April 05, 2019
Package DI Number
10699320202026
Quantity per Package
10
Contains DI Package
00699320202029
Package Discontinue Date
-
Package Status
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 |