Diamatrix

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name: Diamatrix FDA UDI
Generic Name: Ocular hook/spatula/manipulator, reusable FDA UDI
Device Name: Castroviejo Lacrimal Dilator, Unique double sided instrument, Lacrimal Dilator, Size 1 Fine Taper / Size 2 Medium Taper, Diamond knurled handle, 120mm total length, Stainless FDA UDI
Model / Reference: H735 FDA UDI
Description: Castroviejo Lacrimal Dilator, Unique double sided instrument, Lacrimal Dilator, Size 1 Fine Taper / Size 2 Medium Taper, Diamond knurled handle, 120mm total length, Stainless FDA UDI

Identifiers

Primary DI / UDI-DI: 00813059015112 FDA UDI
FDA Product Code: HNQ FDA UDI
GMDN Term: Ocular hook/spatula/manipulator, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Ocular hook/spatula/manipulator, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Diamatrix

Sources (1)

FDA UDI 2dca17c9-2c97-4400-b01d-96b6944ee1eb 33 fields · synced Jun 1, 2026