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Ciliprobe Transsceral Cyclophotocoagulation Probe

FDA UDI

Class II (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Ciliprobe Transsceral Cyclophotocoagulation Probe FDA UDI
Generic Name
Ophthalmic fibreoptic light instrument, single-use FDA UDI
Device Name
Quantel connector FDA UDI
Model / Reference
D4700C FDA UDI
Description
Quantel connector FDA UDI

Identifiers

Primary DI / UDI-DI
10817489025168 FDA UDI
FDA Product Code
LQJ FDA UDI
GMDN Term
Ophthalmic fibreoptic light instrument, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic fibreoptic light instrument, single-use

Ciliprobe Transsceral Cyclophotocoagulation Probe by Katalyst Surgical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic fibreoptic light instrument, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI f55dc4f7-3242-4853-80dd-dd5d606b0dc1 33 fields · synced Jun 8, 2026