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Acclarent Cyclops

FDA UDI

Class II (US FDA UDI)

by Acclarent, Inc.

Identity

Trade Name
ACCLARENT CYCLOPS FDA UDI
Generic Name
Rigid optical nasopharyngoscope FDA UDI
Device Name
ACCLARENT CYCLOPS MULTI-ANGLE ENDOSCOPE FDA UDI
Model / Reference
CYE002 FDA UDI
Description
ACCLARENT CYCLOPS MULTI-ANGLE ENDOSCOPE FDA UDI

Identifiers

Catalog Number
CYE002 FDA UDI
Primary DI / UDI-DI
10705031135659 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Rigid optical nasopharyngoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid optical nasopharyngoscope

Acclarent Cyclops by Acclarent, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical nasopharyngoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acclarent, Inc.

Sources (1)

  • FDA UDI 0c9b00dd-27f1-450d-87f6-c64f808e3291 36 fields · synced Jun 8, 2026