Duns Number:835465063
Device Description: ENDOTRACH TUBE 8229985 5PK 8.5MM EMG FLX
Catalog Number
-
Brand Name
NIM FLEX™
Version/Model Number
8229985
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K925640,K925640
Product Code
ETN
Product Code Name
STIMULATOR, NERVE
Public Device Record Key
bbd9ddbf-759d-433a-8c2c-dcaf5b375e5d
Public Version Date
March 08, 2021
Public Version Number
2
DI Record Publish Date
May 04, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 665 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1575 |
| 3 | A medical device with high risk that requires premarket approval | 6 |
| U | Unclassified | 10 |