General Manual Instrument 113-084

GUDID 00190837079239

T30 Driver

Life Spine, Inc.

Surgical retraction system, reusable
Primary Device ID00190837079239
NIH Device Record Key5c454279-e2cf-441f-8443-e1ac06df6625
Commercial Distribution StatusIn Commercial Distribution
Brand NameGeneral Manual Instrument
Version Model Number113-084
Catalog Number113-084
Company DUNS183641617
Company NameLife Spine, Inc.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100190837079239 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190837079239]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-27
Device Publish Date2019-11-19

On-Brand Devices [General Manual Instrument]

00190837102586Access Chisel
00190837102579Access Chisel
00190837079239T30 Driver

© 2019 FDA.report
This site is not affiliated with or endorsed by the FDA.