CORUS Guide Tube Adapter PD-04-470

GUDID 10852776006512

CORUS Guide Tube Adapter

PROVIDENCE MEDICAL TECHNOLOGY, INC.

Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Orthopaedic implant/instrument depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter Surgical instrument/implant depth limiter
Primary Device ID10852776006512
NIH Device Record Keyda98b8de-7b10-4683-9017-a8c8a1c58b11
Commercial Distribution StatusIn Commercial Distribution
Brand NameCORUS Guide Tube Adapter
Version Model NumberPD-04-470
Catalog NumberPD-04-470
Company DUNS969820245
Company NamePROVIDENCE MEDICAL TECHNOLOGY, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
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
GS100852776006515 [Primary]
GS110852776006512 [Package]
Contains: 00852776006515
Package: Box [1 Units]
In Commercial Distribution

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-09
Device Publish Date2021-03-01

Devices Manufactured by PROVIDENCE MEDICAL TECHNOLOGY, INC.

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