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Diamatrix Ltd

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix Ltd FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Device Name
Stevens Tenotomy Scissors Heavy Model, Straight, 19mm from screw to blunt tips, Ring style handle, 98mm total length, Stainless FDA UDI
Model / Reference
S509 FDA UDI
Description
Stevens Tenotomy Scissors Heavy Model, Straight, 19mm from screw to blunt tips, Ring style handle, 98mm total length, Stainless FDA UDI

Identifiers

Catalog Number
S509 FDA UDI
Primary DI / UDI-DI
00813059017222 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, conventional-hinge, 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intraocular scissors, conventional-hinge, reusable

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

Similar devices

Also classified as Intraocular scissors, conventional-hinge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI c3b24490-fedc-4356-9c43-20df483b805c 34 fields · synced May 30, 2026