Desmarres (16 mm) Stainless Steel Retractor for Laser (non glare)

GUDID 10697660002139

The Desmarres is a retractor intended to retract tissue around the inferior eyelid's incision. The Desmarres has a shaft and its edge is a curved strip. The Desmarres can be used as a backstop to lay down tissue to excise with the laser. It is a smooth instrument that touches the patient's tissue, the shield or the eyelids.

Oculo-Plastik Inc

Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable Hand-held surgical retractor, reusable
Primary Device ID10697660002139
NIH Device Record Keyc8dd6151-7034-4841-9d05-28ccae5c5d38
Commercial Distribution StatusIn Commercial Distribution
Brand NameDesmarres (16 mm) Stainless Steel Retractor for Laser (non glare)
Version Model Number21-316
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
Phone514-381-3292
Emailsales@oculoplastik.com

Device Dimensions

Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter
Width16 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110697660002139 [Primary]

FDA Product Code

GADRetractor

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

[10697660002139]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-25
Device Publish Date2019-11-15

Devices Manufactured by Oculo-Plastik Inc

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