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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
LASEK alcohol well, reusable FDA UDI
Device Name
Camellin Style LASEK 8.0mm Alcohol Well, Flat Handle, Stainless Steel FDA UDI
Model / Reference
14-0200-8.0 FDA UDI
Description
Camellin Style LASEK 8.0mm Alcohol Well, Flat Handle, Stainless Steel FDA UDI

Identifiers

Primary DI / UDI-DI
G223140200800 FDA UDI
FDA Product Code
HNB FDA UDI
GMDN Term
LASEK alcohol well, 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: LASEK alcohol well, reusable

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

Similar devices

Also classified as LASEK alcohol well, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medetz Surgical Instruments

Sources (1)

  • FDA UDI ba65f0f8-22ec-4307-881a-cf6b1dc5f779 34 fields · synced Jun 8, 2026