← Back to catalogue

Eyes Speculum

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
EYES SPECULUM FDA UDI
Generic Name
Eyelid speculum, single-use FDA UDI
Device Name
SOLID BLADE EYES SPECULUM 7.6 MM X 14.7 MM / LENGTH 5 CM / 2 INCH WIDTH 1.1 INCH FDA UDI
Model / Reference
EYES SPECULUM FDA UDI
Description
SOLID BLADE EYES SPECULUM 7.6 MM X 14.7 MM / LENGTH 5 CM / 2 INCH WIDTH 1.1 INCH FDA UDI

Identifiers

Catalog Number
504008 FDA UDI
Primary DI / UDI-DI
B97450400803 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 — 5 Centimeter FDA UDI

Category: Eyelid speculum, single-use

Eyes Speculum 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 81b7bbeb-bbb1-45bf-b58f-d50b59ec77a4 35 fields · synced Jun 8, 2026