General Instrument 2014-0007

GUDID 00190837090210

DRILL, 4.0mm

Life Spine, Inc.

Surgical retraction system, reusable
Primary Device ID00190837090210
NIH Device Record Key290b40eb-6d80-4fa1-bfb9-07b3d4f13fe2
Commercial Distribution StatusIn Commercial Distribution
Brand NameGeneral Instrument
Version Model Number2014-0007
Catalog Number2014-0007
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
GS100190837090210 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190837090210]

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 Instrument]

00190837089467112-495
00190837089450112-490
00190837089337113-954
00190837089320113-131
00190837085148113-118
00190837079536113-117
00190837079529113-116
00190837079512113-103
00190837090227DRILL, 4.5mm
00190837090210DRILL, 4.0mm

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