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Diamatrix

FDA UDI

Class I (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Utrata-Kershner Capsulorhexis Cystotome Forceps, Angled 11.5mm from bend to tip with extremely thin Sharp triangular grasping tips, Diamond knurled handle with Flat, Guide pin stop for tip alignment, 105mm total length, Titanium FDA UDI
Model / Reference
F663T-A FDA UDI
Description
Utrata-Kershner Capsulorhexis Cystotome Forceps, Angled 11.5mm from bend to tip with extremely thin Sharp triangular grasping tips, Diamond knurled handle with Flat, Guide pin stop for tip alignment, 105mm total length, Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
00813059014948 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, 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 soft-tissue manipulation forceps, tweezers-like, reusable

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

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamatrix

Sources (1)

  • FDA UDI 341e6848-adae-4e55-bf92-aa2b6022c09d 33 fields · synced May 30, 2026