Diamatrix Ltd.

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name: Diamatrix Ltd. FDA UDI
Generic Name: Ocular hook/spatula/manipulator, reusable FDA UDI
Device Name: Lester ll Lens Manipulator .2mm Diameter Teardrop shaped tip, Straight Shaft, Round knurled Handle, 118mm total length, Stainless Steel FDA UDI
Model / Reference: H171-S-S FDA UDI
Description: Lester ll Lens Manipulator .2mm Diameter Teardrop shaped tip, Straight Shaft, Round knurled Handle, 118mm total length, Stainless Steel FDA UDI

Identifiers

Catalog Number: H171-S-S FDA UDI
Primary DI / UDI-DI: 00813059016478 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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Ocular hook/spatula/manipulator, reusable

Diamatrix Ltd. 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 143efb25-6c79-47c3-8371-99e7154f3688 34 fields · synced Jun 1, 2026