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Dacrios Opthalmic Knives

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Dacrios Opthalmic Knives FDA UDI
Generic Name
Ophthalmic knife, single-use FDA UDI
Device Name
Dacrios Clear Corneal Knife, 2.2mm, Double Bevel, Angled, Box of 10 FDA UDI
Model / Reference
D3522 FDA UDI
Description
Dacrios Clear Corneal Knife, 2.2mm, Double Bevel, Angled, Box of 10 FDA UDI

Identifiers

Catalog Number
D3522 FDA UDI
Primary DI / UDI-DI
00813059018915 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Ophthalmic knife, 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 2.2 Millimeter FDA UDI

Category: Ophthalmic knife, single-use

Dacrios Opthalmic Knives by Diamatrix — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic knife, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI 62da2c41-08c7-4a4f-bf17-aa70227fae60 36 fields · synced Jun 8, 2026