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Symblepharon Ring 20 Mm

FDA UDI

Class II (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name
SYMBLEPHARON RING 20 MM FDA UDI
Generic Name
Symblepharon ring, synthetic FDA UDI
Device Name
SYMBLEPHARON RING 20 MM FDA UDI
Model / Reference
S6.2420 FDA UDI
Description
SYMBLEPHARON RING 20 MM FDA UDI

Identifiers

Primary DI / UDI-DI
13700773724915 FDA UDI
FDA Product Code
HQN FDA UDI
GMDN Term
Symblepharon ring, synthetic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.3130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Symblepharon ring, synthetic

Symblepharon Ring 20 Mm by Fci S A S Fci 20 22 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Symblepharon ring, synthetic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fci S A S Fci 20 22

Sources (1)

  • FDA UDI 98e47bb1-3a4b-45fb-934e-79deb1560477 33 fields · synced May 30, 2026