RELIANCE C 48365304

GUDID 07613327008173

GENERAL TRIAL

Stryker Corporation

Spinal implant trial
Primary Device ID07613327008173
NIH Device Record Keyc184d320-50f2-41e4-8233-29b7e406732d
Commercial Distribution StatusIn Commercial Distribution
Brand NameRELIANCE C
Version Model Number48365304
Catalog Number48365304
Company DUNS149183167
Company NameStryker Corporation
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Height4 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327008173 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327008173]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-10
Device Publish Date2019-12-02

On-Brand Devices [RELIANCE C]

07613327269956FLAT TAMP
07613327008241CURVED TAMP
07613327008135CONTAINER
07613327270044GENERAL TRIAL
07613327269932GENERAL TRIAL
07613327269918GENERAL TRIAL
07613327008234GENERAL TRIAL
07613327008227GENERAL TRIAL
07613327008210GENERAL TRIAL
07613327008203GENERAL TRIAL
07613327008180GENERAL TRIAL
07613327008173GENERAL TRIAL
07613327269857PARALLEL PIN DISTRACTOR
07613327269925COBB
07613327008142PADDLE DISTRACTOR
07613327270136DOUBLE-SIDED RASP
07613327269949DOUBLE-SIDED RASP
07613327269901DOUBLE-SIDED RASP
07613327269895DOUBLE-SIDED RASP
07613327269888DOUBLE-SIDED RASP
07613327269871DOUBLE-SIDED RASP
07613327269864DOUBLE-SIDED RASP
07613327008166DOUBLE-SIDED RASP
07613327008159DOUBLE-SIDED RASP

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