ACTU8 Tewari (T2) Forceps VS0742.25

GUDID B384VS074225

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 IDB384VS074225
NIH Device Record Key5dcf5a68-8a6a-49a8-9eeb-90699553c747
Commercial Distribution StatusIn Commercial Distribution
Brand NameACTU8 Tewari (T2) Forceps
Version Model Number25ga
Catalog NumberVS0742.25
Company DUNS080375891
Company NameVORTEX SURGICAL, LLC
Device Count1
DM Exemptfalse
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
HIBCCB384VS074225 [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 Tewari (T2) Forceps]

B384VS074225Ophthalmic Forceps
B384VS074221Ophthalmic Forceps

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