Castroviejo Suturing Forceps (0.9 mm), refurb.

GUDID 10697660003488

Stainless Steel Suturing Forceps (non glare), refurbished

Oculo-Plastik Inc

Surgical soft-tissue manipulation forceps, alligator, reusable
Primary Device ID10697660003488
NIH Device Record Keybbd1de08-81f6-4c2b-ae21-b6f35cf6ad97
Commercial Distribution Discontinuation2022-03-24
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCastroviejo Suturing Forceps (0.9 mm), refurb.
Version Model Number25-109R
Company DUNS257382580
Company NameOculo-Plastik 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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com
Phone514-381-3292
Emailsales@oculoplastik.com

Device Dimensions

Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter
Width0.9 Millimeter
Length10 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110697660003488 [Primary]

FDA Product Code

GENForceps, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


[10697660003488]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-03-25
Device Publish Date2019-11-21

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