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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
Lieberman Microfinger & Spatula, Unique double sided instrument, Lieberman Microfinger Unique C-Shaped Chopper with blunt tip ~ .5mm wide flat spatula, Both Angled 10mm from bend to tip, Intended to be used in the left hand, Diamatrix Signature Feather-Series round handle, 142mm total length, Titanium/Stainless FDA UDI
Model / Reference
H562-L-D FDA UDI
Description
Lieberman Microfinger & Spatula, Unique double sided instrument, Lieberman Microfinger Unique C-Shaped Chopper with blunt tip ~ .5mm wide flat spatula, Both Angled 10mm from bend to tip, Intended to be used in the left hand, Diamatrix Signature Feather-Series round handle, 142mm total length, Titanium/Stainless FDA UDI

Identifiers

Catalog Number
H562-L-D FDA UDI
Primary DI / UDI-DI
00813059018311 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

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: Ocular hook/spatula/manipulator, reusable

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

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI a394e197-669c-4992-b474-d22b649cd347 35 fields · synced Jun 8, 2026