Duns Number:025460908
Device Description: PAD,EYE,LARGE,2 1/8"X2 5/8",STERILE,LF
Catalog Number
NON21601
Brand Name
Medline
Version/Model Number
NON21601
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
HMP
Product Code Name
PAD, EYE
Public Device Record Key
0f025005-f61f-4415-9924-0f607e62aa15
Public Version Date
January 27, 2021
Public Version Number
1
DI Record Publish Date
January 19, 2021
Package DI Number
40080196749189
Quantity per Package
600
Contains DI Package
30080196749182
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 | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |