03816446

GUDID 07612334216281

4TH BLADE STRAIGHT LONG

SYNTHES (U.S.A.) LP

Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable
Primary Device ID07612334216281
NIH Device Record Keyf7dcb2cf-d7f5-46c0-8bfc-b0c9d06905c2
Commercial Distribution StatusIn Commercial Distribution
Version Model Number03.816.446
Catalog Number03816446
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS107612334216281 [Direct Marking]
GS110705034821733 [Primary]
GS110705034821733 [Primary]
GS110705034821733 [Primary]
GS110705034821733 [Primary]
GS110705034821733 [Primary]
GS110705034821733 [Primary]
GS110705034821733 [Primary]
GS110705034821733 [Primary]

FDA Product Code

GADRETRACTOR
GADRETRACTOR
GADRETRACTOR
GADRETRACTOR
GADRETRACTOR
GADRETRACTOR
GADRETRACTOR
GADRETRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


[07612334216281]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-09
Device Publish Date2020-10-30

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

07612334216298 - NA2020-11-09 STYLET Ø 4 MM
07612334216168 - NA2020-11-09 4TH BLADE CURVED NARROW SHORT
07612334216175 - NA2020-11-09 4TH BLADE CURVED NARROW MED
07612334216182 - NA2020-11-09 4TH BLADE CURVED NARROW LONG
07612334216199 - NA2020-11-09 4TH BLADE CURVED WIDE SHORT
07612334216205 - NA2020-11-09 4TH BLADE CURVED WIDE MEDIUM
07612334216212 - NA2020-11-09 4TH BLADE CURVED WIDE LONG
07612334216267 - NA2020-11-09 4TH BLADE STRAIGHT SHORT

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.