SD520002

GUDID H980SD5200020

SAW BLADE 34X6.4/2.9X0.6MM TRAPEZOID F/RECIP SAW

SYNTHES (U.S.A.) LP

Reciprocating surgical saw blade, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable Surgical saw blade, reciprocating, reusable
Primary Device IDH980SD5200020
NIH Device Record Keyd0c6cddc-407f-45f6-8127-7536b075b253
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberSD520.002
Catalog NumberSD520002
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
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 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

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110887587005492 [Primary]
HIBCCH980SD5200020 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWEINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


[H980SD5200020]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-30

Devices Manufactured by SYNTHES (U.S.A.) LP

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H679022221160 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/16MM
H679022221180 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/18MM
H679022221200 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/20MM
H679022221220 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/22MM
H679022221240 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/24MM
H679022221260 - NA2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/26MM

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