Connor Wand

GUDID 05056785303343

BLINK MEDICAL LIMITED

Ophthalmic surgical probe, single-use
Primary Device ID05056785303343
NIH Device Record Key462c31e2-be3f-4cf8-80b1-bc9bc95bdc2d
Commercial Distribution StatusIn Commercial Distribution
Brand NameConnor Wand
Version Model Number41-4013BNS
Company DUNS738288096
Company NameBLINK MEDICAL LIMITED
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS105056785303336 [Primary]
GS105056785303343 [Package]
Contains: 05056785303336
Package: [20 Units]
In Commercial Distribution

FDA Product Code

HNDSpatula, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


[05056785303343]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-03
Device Publish Date2026-01-26

On-Brand Devices [Connor Wand]

0506074555487441-4013
0505678530334341-4013BNS

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