Primary Device ID | 00840096206340 |
NIH Device Record Key | 8dcfaf87-849e-4b5e-8c3e-d54172b5e1d6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 23ga ISOCLEAN™ Serrated Forceps, Curved Shaft, Gold |
Version Model Number | 3451C-M23G |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840096206340 [Primary] |
HNR | Forceps, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840096206340]
Moist Heat or Steam Sterilization
[00840096206340]
Moist Heat or Steam Sterilization
[00840096206340]
Moist Heat or Steam Sterilization
[00840096206340]
Moist Heat or Steam Sterilization
[00840096206340]
Moist Heat or Steam Sterilization
[00840096206340]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-04-04 |
Device Publish Date | 2020-05-26 |
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