Bores Axis Marker Titanium AS3-001T

GUDID 08175700106696

Bores Axis Marker Titanium

AURORA SURGICAL, LLC

Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable Ophthalmic angular gauge, reusable
Primary Device ID08175700106696
NIH Device Record Key06c59aeb-6f52-4425-a641-6888314aa363
Commercial Distribution StatusIn Commercial Distribution
Brand NameBores Axis Marker Titanium
Version Model NumberAS3-001T
Catalog NumberAS3-001T
Company DUNS968368832
Company NameAURORA SURGICAL, LLC
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 Batchfalse
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

Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com
Phone7278213303
Emailinfo@aurorasurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108175700106696 [Primary]

FDA Product Code

HLFDevice, Measuring, Lens Radius, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

[08175700106696]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-22
Device Publish Date2022-11-14

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08175700157025 - Punches2024-03-19 Meyerhoefer Chalazion Curette, Size 2-2.0mm
08175700157032 - Punches2024-03-19 Meyerhoefer Chalazion Curette, Size 3-2.5mm
08175700157049 - Punches2024-03-19 Meyerhoefer Chalazion Curette, Size 4-3.5mm
08175700157506 - Punches2024-03-19 Wilder Lens Loop With Serrations
08175700157513 - Punches2024-03-19 New Orleans Lens Loop
08175700157520 - Punches2024-03-19 Kirby Lens Loop and Expressor
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