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Lester Lens Pusher

FDA UDI

Class I (US FDA UDI)

by Medetz Surgical Instruments

Identity

Trade Name
Lester Lens Pusher FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Device Name
Lester Lens Pusher Hour Glass Tip, Straight, With Guard OL 120mm (4 3/4") FDA UDI
Model / Reference
11-9460 FDA UDI
Description
Lester Lens Pusher Hour Glass Tip, Straight, With Guard OL 120mm (4 3/4") FDA UDI

Identifiers

Primary DI / UDI-DI
G2231194600 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Ophthalmic surgical probe, 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: Ophthalmic surgical probe, reusable

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

Similar devices

Also classified as Ophthalmic surgical probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d53137cd-b63c-41cc-a81e-8b27e13fcb45 34 fields · synced Jun 8, 2026