Primary Device ID | 00840096203936 |
NIH Device Record Key | 5babbaf0-5f3d-4ad5-aea4-26b00a9b64aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | #4- Spatula Dissector, Small, 1.5mm |
Version Model Number | N083-080 |
Company DUNS | 007883297 |
Company Name | KATALYST SURGICAL LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840096203936 [Primary] |
HTE | Elevator |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840096203936]
Moist Heat or Steam Sterilization
[00840096203936]
Moist Heat or Steam Sterilization
[00840096203936]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-19 |
Device Publish Date | 2020-05-11 |