AUFRICHT RETRACTOR 207-290

GUDID 00192896025653

AUFRICHT RETRACTOR FENESTRATED BLADE

SONTEC INSTRUMENTS, INC.

Hand-held surgical retractor, reusable
Primary Device ID00192896025653
NIH Device Record Keyd816f407-1096-4d73-8321-b9459e08d1d7
Commercial Distribution StatusIn Commercial Distribution
Brand NameAUFRICHT RETRACTOR
Version Model Number207-290
Catalog Number207-290
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, 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 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) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length6.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896025653 [Primary]

FDA Product Code

GADRETRACTOR
KALRetractor, Ent

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896025653]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-11-19
Device Publish Date2018-09-14

On-Brand Devices [AUFRICHT RETRACTOR]

00192896090330AUFRICHT RETRACTOR SOLID BLADE
00192896025745AUFRICHT RETRACTOR SOLID BLADE BLACK NON-REFLECTIVE FINISH
00192896025738AUFRICHT RETRACTOR ILLUMINATED SOLID BLADE
00192896025660AUFRICHT RETRACTOR SOLID BLADE
00192896025653AUFRICHT RETRACTOR FENESTRATED BLADE
00192896116009Aufricht Nasal Retractor Illuminated

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