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Capsulorrhexis Forceps

FDA UDI

Class I (US FDA UDI)

by Aurora Surgical, Llc

Identity

Trade Name
Capsulorrhexis Forceps FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Capsulorrhexis Forceps, Kawai Type, Cystotome Tip Serrated Grove, Incremental Marks at 2.5, 5.0 &7.5mm, 23g Titanium Squeeze Handle FDA UDI
Model / Reference
AS7-124T FDA UDI
Description
Capsulorrhexis Forceps, Kawai Type, Cystotome Tip Serrated Grove, Incremental Marks at 2.5, 5.0 &7.5mm, 23g Titanium Squeeze Handle FDA UDI

Identifiers

Catalog Number
AS7-124T FDA UDI
Primary DI / UDI-DI
08175700122917 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

No

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

No

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

Capsulorrhexis Forceps by Aurora Surgical, Llc — 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

Sources (1)

  • FDA UDI 80bfc03f-e363-41e2-bd8c-e8cf45fb9b16 34 fields · synced Jun 6, 2026