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Flieringa Scleral Fixation Ring

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
FLIERINGA SCLERAL FIXATION RING FDA UDI
Generic Name
Flieringa ophthalmic ring FDA UDI
Device Name
FLIERINGA SCLERAL FIXATION RING FDA UDI
Model / Reference
10-3140 FDA UDI
Description
FLIERINGA SCLERAL FIXATION RING FDA UDI

Identifiers

Catalog Number
10-3140 FDA UDI
Primary DI / UDI-DI
00192896088399 FDA UDI
FDA Product Code
HNI FDA UDI
GMDN Term
Flieringa ophthalmic ring 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 14 Millimeter FDA UDI

Category: Flieringa ophthalmic ring

Flieringa Scleral Fixation Ring by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flieringa ophthalmic ring.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0da2b31d-a9f7-4223-9a72-826a52b6445e 36 fields · synced Jun 1, 2026