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Medetz Surgical Instruments

FDA UDI

Class I (US FDA UDI)

by Medetz Surgical Instruments

Identity

Trade Name
Medetz Surgical Instruments FDA UDI
Generic Name
Corneoscleral punch FDA UDI
Device Name
Kelly decemet membrane punch FDA UDI
Model / Reference
11-1687a FDA UDI
Description
Kelly decemet membrane punch FDA UDI

Identifiers

Primary DI / UDI-DI
G223110687A0 FDA UDI
FDA Product Code
HNJ FDA UDI
GMDN Term
Corneoscleral punch 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Corneoscleral punch

Medetz Surgical Instruments by Medetz Surgical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneoscleral punch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d15e7b71-d67a-4c01-b9a6-3db6793aa1f1 34 fields · synced May 30, 2026