Duns Number:080361159
Device Description: DRAPE, TRANSPARENT INTUBATION, 56"X70", AAMI LEVEL 2, 1" ADHESIVE CENTERED ON LONG SIDE OF DRAPE, TRANSPARENT INTUBATION, 56"X70", AAMI LEVEL 2, 1" ADHESIVE CENTERED ON LONG SIDE OF DRAPE, 1EA/BG, 100BG/CS
Catalog Number
-
Brand Name
ASP MEDICAL
Version/Model Number
DRAPE5670
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
PUI
Product Code Name
Drape, Surgical, Exempt
Public Device Record Key
2c7fc311-eca7-4d3e-aab7-33bcdf554ddf
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
April 02, 2021
Package DI Number
10840216108742
Quantity per Package
100
Contains DI Package
00840216108745
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 | 1046 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 23 |
| U | Unclassified | 2 |