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: Westcott Stitch Scissors, Curved, Very Sharp Pointed tips, 19mm from pivot to tip, Serrated Scissor-Action Handle, 115mm total length, Stainless FDA UDI
Model / Reference: S405-S FDA UDI
Description: Westcott Stitch Scissors, Curved, Very Sharp Pointed tips, 19mm from pivot to tip, Serrated Scissor-Action Handle, 115mm total length, Stainless FDA UDI

Identifiers

Catalog Number: S405-S FDA UDI
Primary DI / UDI-DI: 00813059016850 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

Similar devices

Also classified as Ocular hook/spatula/manipulator, reusable.

CARLSON DSEK SMOOTHER — DAUD JEE MFG. CO · Class I
57150 Spatula, Model Giessen — Bausch & Lomb GmbH · Class I
Rumex — Rumex International Co. · Class I
Ophthalmic Spatula — CILITA Ltd. · Class I
Rumex — Rumex International Co. · Class I
Sklar — Sklar Corporation · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Walcott Rx Products — Walcott Rx Product Inc · Class I

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

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

Manufacturer

Manufacturer: Diamatrix

Sources (1)

FDA UDI 0857a98e-488b-4549-8f22-4b02516b9feb 35 fields · synced May 30, 2026