Flex Curved Laser Probe, 23g Nidek

FDA UDI

Class II (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name: FLEX CURVED LASER PROBE, 23G NIDEK FDA UDI
Generic Name: Ophthalmic laser system beam guide FDA UDI
Device Name: FLEX CURVED LASER PROBE, 23G NIDEK FDA UDI
Model / Reference: S9.1214.23 FDA UDI
Description: FLEX CURVED LASER PROBE, 23G NIDEK FDA UDI

Identifiers

Primary DI / UDI-DI: 13700773720429 FDA UDI
FDA Product Code: HQB FDA UDI
GMDN Term: Ophthalmic laser system beam guide FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4690 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic laser system beam guide

Flex Curved Laser Probe, 23g Nidek by Fci S A S Fci 20 22 — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Ophthalmic laser system beam guide.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Fci S A S Fci 20 22

Sources (1)

FDA UDI 3335e28a-c754-4dff-a55e-22e537fef358 33 fields · synced May 30, 2026