ACTU8 Adaptive Forceps VS0740.23

GUDID B384VS0740231

Ophthalmic Forceps

VORTEX SURGICAL, LLC

Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use Ophthalmic soft-tissue manipulation forceps, tweezers-like, single-use
Primary Device IDB384VS0740231
NIH Device Record Keyc8d666fa-e7fd-48a4-a092-3b9d46a1ab24
Commercial Distribution StatusIn Commercial Distribution
Brand NameACTU8 Adaptive Forceps
Version Model Number23ga
Catalog NumberVS0740.23
Company DUNS080375891
Company NameVORTEX SURGICAL, LLC
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB384VS0740231 [Primary]

FDA Product Code

HNRForceps, Ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-10-05
Device Publish Date2018-03-15

On-Brand Devices [ACTU8 Adaptive Forceps]

B384VS0740251Ophthalmic Forceps
B384VS0740231Ophthalmic Forceps

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.