SynFrame 03609050

GUDID H981036090500

SYNFRAME RETRACTOR-OBLIQUE 23MM WIDTH/100MM

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 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 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 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 IDH981036090500
NIH Device Record Keydbfe336e-63f4-407f-9a73-26277c5d930d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSynFrame
Version Model Number03.609.050
Catalog Number03609050
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
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
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
GS110705034713120 [Primary]
HIBCCH981036090500 [Secondary]

FDA Product Code

GADRETRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


[H981036090500]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-05-10
Device Publish Date2016-12-31

On-Brand Devices [SynFrame]

H9816900800SYNFRAME AUXILIARY INSTRUMENT SET GRAPHIC CASE
H9816900290SYNFRAME BONE LEVER GRAPHIC CASE
H9816900180SYNFRAME RETRACTOR GRAPHIC CASE
H9816900170SYNFRAME GRAPHIC CASE
07611819110168SYNFRAME BONE LEVER- 18MM WIDTH/190MM
07611819110151SYNFRAME BONE LEVER- 18MM WIDTH/170MM
07611819099548SYNFRAME RETRACTOR 180MM
07611819099531SYNFRAME RETRACTOR 160MM
07611819099517SYNFRAME RETRACTOR 120MM
07611819099500SYNFRAME RETRACTOR 100MM
07611819099494SYNFRAME RETRACTOR 80MM
07611819099487SYNFRAME RETRACTOR 60MM
H981036090580SYNFRAME RETRACTOR-OBLIQUE 23MM WIDTH/180MM
H981036090560SYNFRAME RETRACTOR-OBLIQUE 23MM WIDTH/160MM
H981036090540SYNFRAME RETRACTOR-OBLIQUE 23MM WIDTH/140MM
H981036090520SYNFRAME RETRACTOR-OBLIQUE 23MM WIDTH/120MM
H981036090500SYNFRAME RETRACTOR-OBLIQUE 23MM WIDTH/100MM

Trademark Results [SynFrame]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SYNFRAME
SYNFRAME
78943760 3268141 Live/Registered
DEPUY SYNTHES, INC.
2006-08-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.