Curved Connection Rod

GUDID 06912547394648

Shandong Weigao Orthopaedic Device Co., Ltd.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID06912547394648
NIH Device Record Keyeec92b67-63d4-40f0-af9e-fe766f68f8d7
Commercial Distribution StatusIn Commercial Distribution
Brand NameCurved Connection Rod
Version Model Number803805130
Company DUNS545249039
Company NameShandong Weigao Orthopaedic Device Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106912547394648 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWPAppliance, Fixation, Spinal Interlaminal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[06912547394648]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-12-12

On-Brand Devices [Curved Connection Rod]

06912547394662803805150
06912547394655803805140
06912547394648803805130
06912547394631803805120
06912547394624803805110
06912547394617803805105
06912547394600803805100
06912547394594803805095
06912547394587803805090
06912547394570803805085
06912547394563803805080
06912547394556803805075
06912547394549803805070
06912547394532803805065
06912547394525803805060
06912547394518803805055
06912547394501803805050
06912547394495803805045
06912547394488803805040
06912547394471803805035
06912547394464803805030
06912547394457803805025

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