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Meyco

FDA UDI

Class I (US FDA UDI)

by Anton Meyer & Co. AG

Identity

Trade Name
Meyco FDA UDI
Generic Name
Ophthalmic knife, reusable FDA UDI
Device Name
diamond knife for eye surgery FDA UDI
Model / Reference
ME131 FDA UDI
Description
diamond knife for eye surgery FDA UDI

Identifiers

Primary DI / UDI-DI
05060518820076 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Ophthalmic knife, 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic knife, reusable

Meyco by Anton Meyer & Co. AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic knife, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 239c54b3-7edb-40af-b21a-9dee951c18cc 34 fields · synced May 30, 2026