Duns Number:015272206
Device Description: Foerster capsulotomy knife, 10 1/2'', for sepatarion of the spherical contracture, V-shape Foerster capsulotomy knife, 10 1/2'', for sepatarion of the spherical contracture, V-shaped cutting edge, round handle
Catalog Number
39-360
Brand Name
Ambler Surgical
Version/Model Number
Foerster capsulotomy knife
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
-
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
-
Product Code
EMF
Product Code Name
KNIFE, SURGICAL
Public Device Record Key
cc992888-017c-4bb9-9d15-3640752aa710
Public Version Date
June 22, 2021
Public Version Number
2
DI Record Publish Date
January 04, 2021
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 | 14984 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3118 |