5405

GUDID 30818255011211

Round Silicone Sponge 5.0mm x 80mm

MICROVISION, INC.

Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable Scleral buckling device, non-bioabsorbable
Primary Device ID30818255011211
NIH Device Record Keyf3d0a26e-edcf-4ffa-81cf-5b37ab4c0b0d
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberStyle 505
Catalog Number5405
Company DUNS013486803
Company NameMICROVISION, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter
Length80 Millimeter
Outer Diameter5 Millimeter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS110818255011217 [Primary]
GS130818255011211 [Package]
Contains: 10818255011217
Package: Carton [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HQXImplant, Orbital, Extra-Ocular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-12-22
Device Publish Date2017-12-22

Devices Manufactured by MICROVISION, INC.

30818255011198 - NA2021-12-22 Round Silicone Sponge 3.0mm x 80mm
30818255011204 - NA2021-12-22 Round Silicone Sponge 4.0mm x 80mm
30818255011211 - NA2021-12-22Round Silicone Sponge 5.0mm x 80mm
30818255011211 - NA2021-12-22 Round Silicone Sponge 5.0mm x 80mm
30818255011228 - NA2021-12-22 Oval Silicone Sponge 3.0mm x 5.0mm x 100mm
30818255011235 - NA2021-12-22 Oval Silicone Sponge 5.5mm x 7.5mm x 80mm
30818255011327 - NA2021-12-22 Concave Silicone Tire 7.0mm, 2.5mm groove
30818255011334 - NA2021-12-22 Concave Silicone Tire 9.0mm, 2.5mm groove
30818255011372 - NA2021-12-22 Asymmetrical Silicone Tire 7.0mm, 2.5mm groove

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