← Back to catalogue

Diamatrix Ltd.

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix Ltd. FDA UDI
Generic Name
Eyelid speculum, reusable FDA UDI
Device Name
Dr. Dees 14mm Animal RIGHT Eye Speculum with unique third eyelid re-tractor on bottom blade, .035'' Stainless Wire, Designed for large animals, 18mm Blade Spread, 39mm Overall Length FDA UDI
Model / Reference
AW-224-14R FDA UDI
Description
Dr. Dees 14mm Animal RIGHT Eye Speculum with unique third eyelid re-tractor on bottom blade, .035'' Stainless Wire, Designed for large animals, 18mm Blade Spread, 39mm Overall Length FDA UDI

Identifiers

Catalog Number
AW-224-14R FDA UDI
Primary DI / UDI-DI
00813059018861 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

Category: Eyelid speculum, reusable

Diamatrix Ltd. by Diamatrix — 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

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

Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI 5e9aa6a6-a0ad-4887-b99a-23136cca608e 35 fields · synced May 31, 2026