Surgical depth gauge, single-use S1.1289U

GUDID 53760087120252

A sterile surgical instrument designed to accurately determine the depth of a recess (usually a drilled hole). It typically consists of a moveable (sliding) centerpiece (a prong), the tip of which is inserted into the recess; when the tip makes contact with the bottom a reading is visually taken from a scale marked on the side of the device. It is often used to measure the depth of holes being drilled in bone so that the surgeon can determine the length of the bone screw to be used. It is made of corrosive resistant materials [e.g., stainless steel, titanium (Ti), plastics]. This is a single-use device.

FCI S A S FCI 20 22

Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use Surgical depth gauge, single-use
Primary Device ID53760087120252
NIH Device Record Key3b676a1a-e26e-4597-a6f6-dcf069a011e2
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurgical depth gauge, single-use
Version Model NumberSIZER FOR SELF-RETAINING BICANALICULUS INTUBATION
Catalog NumberS1.1289U
Company DUNS763408366
Company NameFCI S A S FCI 20 22
Device Count5
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com
Phone800-932-4202
Emailorders@fci-ophthalmics.com

Device Dimensions

Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter
Length80 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103760087120257 [Primary]
GS153760087120252 [Unit of Use]

FDA Product Code

HNLProbe, Lachrymal

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


[53760087120252]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-16
Device Publish Date2020-03-06

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