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Diamatrix

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix FDA UDI
Generic Name
Ophthalmic implant handling forceps, reusable FDA UDI
Device Name
Implant Removal Forceps, Flat serrated jaws with sharp activation pin on bottom jaw, Scissor-action Flat serrated handle, 120mm Overall Length, Stainless Steel FDA UDI
Model / Reference
F355S FDA UDI
Description
Implant Removal Forceps, Flat serrated jaws with sharp activation pin on bottom jaw, Scissor-action Flat serrated handle, 120mm Overall Length, Stainless Steel FDA UDI

Identifiers

Catalog Number
F355S FDA UDI
Primary DI / UDI-DI
00813059017079 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic implant handling forceps, 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: Ophthalmic implant handling forceps, reusable

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

Similar devices

Also classified as Ophthalmic implant handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI 60449aac-5ea3-4525-bb6f-1ab3805d1690 35 fields · synced May 30, 2026