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Fine/Thornton Fixation Ring With Swivel, 13mm Diameter, 11mm Opening, Titanium

FDA UDI

Class I (US FDA UDI)

by Aurora Surgical, Llc

Identity

Trade Name
Fine/Thornton Fixation Ring With Swivel, 13mm Diameter, 11mm Opening, Titanium FDA UDI
Generic Name
Eyeball fixation instrument, reusable FDA UDI
Device Name
Fine/Thornton Fixation Ring With Swivel, 13mm Diameter, 11mm Opening, Titanium FDA UDI
Model / Reference
AS1-350T FDA UDI
Description
Fine/Thornton Fixation Ring With Swivel, 13mm Diameter, 11mm Opening, Titanium FDA UDI

Identifiers

Catalog Number
AS1-350T FDA UDI
Primary DI / UDI-DI
08175700105514 FDA UDI
FDA Product Code
HNH FDA UDI
GMDN Term
Eyeball fixation instrument, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Eyeball fixation instrument, reusable

Fine/Thornton Fixation Ring With Swivel, 13mm Diameter, 11mm Opening, Titanium by Aurora Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Eyeball fixation instrument, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0dc940b7-b000-4631-a966-7708e765f3df 34 fields · synced May 30, 2026