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Eye Specula

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
EYE SPECULA FDA UDI
Generic Name
Eyelid speculum, single-use FDA UDI
Device Name
EYE SPECULA HOLLOW 15MM 1-1/2 INCH LENTH FDA UDI
Model / Reference
EYE SPECULA HOLLOW FDA UDI
Description
EYE SPECULA HOLLOW 15MM 1-1/2 INCH LENTH FDA UDI

Identifiers

Catalog Number
ES500P FDA UDI
Primary DI / UDI-DI
B974ES500P0 FDA UDI
FDA Product Code
HNC FDA UDI
GMDN Term
Eyelid speculum, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 1.5 Inch FDA UDI

Category: Eyelid speculum, single-use

Eye Specula by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eyelid speculum, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 80e9ace7-b2c2-434b-93ca-90bda7955c36 35 fields · synced May 30, 2026