CASPAR LUMBAR SPECULA 416-821

GUDID 00192896079403

CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED

SONTEC INSTRUMENTS, INC.

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 ID00192896079403
NIH Device Record Key88a62cff-c5ce-46d7-bbe0-537b16584419
Commercial Distribution StatusIn Commercial Distribution
Brand NameCASPAR LUMBAR SPECULA
Version Model Number416-821
Catalog Number416-821
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
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Width18 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter
Length45 Millimeter
Width18 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896079403 [Primary]

FDA Product Code

FFORETRACTOR, SELF-RETAINING
FXESpeculum, Non-Illuminated

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896079403]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-03-11
Device Publish Date2018-09-20

On-Brand Devices [CASPAR LUMBAR SPECULA]

00192896079441CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
00192896079434CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
00192896079427CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
00192896079410CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
00192896079403CASPAR LUMBAR SPECULA NON-REFLECTIVE BLACK ANNODIZED COATED
00192896096363CASPAR LUMBAR SPECULA BLACK ANODIZED COATED
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