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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
Eyelid speculum, reusable FDA UDI
Device Name
Barraquer Eye Speculum, .039 Stainless Wire, 14mm Solid Blades Rounded, Nasal Approach, 18mm Blade Spread, 40mm Overall Length FDA UDI
Model / Reference
m11-3095s FDA UDI
Description
Barraquer Eye Speculum, .039 Stainless Wire, 14mm Solid Blades Rounded, Nasal Approach, 18mm Blade Spread, 40mm Overall Length FDA UDI

Identifiers

Primary DI / UDI-DI
G223M113095S0 FDA UDI
FDA Product Code
HNC FDA UDI
GMDN Term
Eyelid speculum, 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

No

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: Eyelid speculum, 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 Eyelid speculum, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f757b09-ef6d-4523-9327-ef0976a9d719 34 fields · synced Jun 1, 2026