← Back to catalogue

Chandelier 25g

FDA UDI

Class II (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name
CHANDELIER 25G FDA UDI
Generic Name
Ophthalmic fibreoptic light instrument, single-use FDA UDI
Device Name
CHANDELIER 25G FDA UDI
Model / Reference
S9.2301.25 FDA UDI
Description
CHANDELIER 25G FDA UDI

Identifiers

Primary DI / UDI-DI
13700773700292 FDA UDI
510(k) Number
K121187 FDA UDI
FDA Product Code
HQF FDA UDI
HQB FDA UDI
MPA 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
886.4690 FDA UDI
876.1500 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic fibreoptic light instrument, single-use

Chandelier 25g 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 Ophthalmic fibreoptic light instrument, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fci S A S Fci 20 22

Sources (1)

  • FDA UDI d0821657-f163-4f93-a81f-234fbe78b179 34 fields · synced Jun 8, 2026