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Symmetry Guyton-Park

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Guyton-Park FDA UDI
Generic Name
Eyelid speculum, reusable FDA UDI
Device Name
Symmetry® Speculum, Guyton-Park, Solid, 14.0 mm Blade, 3 3/8 in FDA UDI
Model / Reference
60-1938 FDA UDI
Description
Symmetry® Speculum, Guyton-Park, Solid, 14.0 mm Blade, 3 3/8 in FDA UDI

Identifiers

Catalog Number
60-1938 FDA UDI
Primary DI / UDI-DI
00887482111147 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 14 Millimeter FDA UDI
Length — 3.375 Inch FDA UDI

Category: Eyelid speculum, reusable

Symmetry Guyton-Park by Symmetry Surgical Inc. — 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 fa1827ba-91a9-4b0b-8002-8d7d93febd3b 36 fields · synced May 30, 2026