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Alcon Grieshaber MONARCH

FDA UDI

Class I (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
Alcon Grieshaber MONARCH FDA UDI
Generic Name
Ophthalmic implant handling forceps, reusable FDA UDI
Device Name
MONARCHTM Loading Forceps FDA UDI
Model / Reference
560.01 FDA UDI
Description
MONARCHTM Loading Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
07612717057470 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic implant handling forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic implant handling forceps, reusable

Alcon Grieshaber MONARCH by Alcon Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic implant handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (1)

  • FDA UDI b3a90e2a-ab70-4416-8745-1058d64c2919 34 fields · synced Jun 1, 2026