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Ophthalmic Scissors

FDA UDI

Class I (US FDA UDI)

by Medetz Surgical Instruments

Identity

Trade Name
Ophthalmic Scissors FDA UDI
Generic Name
Ophthalmic strabismus scissors, reusable FDA UDI
Device Name
Strabismus Scissor Ribbon Type,Straight OL110mm(4 3/8") FDA UDI
Model / Reference
11-3570 FDA UDI
Description
Strabismus Scissor Ribbon Type,Straight OL110mm(4 3/8") FDA UDI

Identifiers

Primary DI / UDI-DI
G2231135700 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Ophthalmic strabismus scissors, 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 strabismus scissors, reusable

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

Similar devices

Also classified as Ophthalmic strabismus scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca07f5e5-c111-456c-b1e6-69174a3644e5 34 fields · synced May 30, 2026