Typenex Medical 098309

GUDID 02816901022540

LEONI FIBER OPTICS, INC.

General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system General/multiple surgical diode laser system
Primary Device ID02816901022540
NIH Device Record Key15f09f0a-d4ec-4269-84fd-8037818fc7ab
Commercial Distribution StatusIn Commercial Distribution
Brand NameTypenex Medical
Version Model NumberNV0615
Catalog Number098309
Company DUNS039281260
Company NameLEONI FIBER OPTICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816901022542 [Primary]
GS101816901022541 [Package]
Contains: 00816901022542
Package: [5 Units]
In Commercial Distribution
GS102816901022540 [Package]
Contains: 01816901022541
Package: [2 Units]
In Commercial Distribution

FDA Product Code

GEXPowered laser surgical instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-02
Device Publish Date2021-06-24

On-Brand Devices [Typenex Medical]

01816901022671NV0615
01816901022664NV0626
01816901022589NV0632
01816901022572NV0633
01816901022558NV0635
02816901023035NV0627
02816901022540NV0615
01816901023708NV0635
01816901023470NV0633

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