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Capsulotomy Scissors

FDA UDI

Class I (US FDA UDI)

by Aurora Surgical, Llc

Identity

Trade Name
Capsulotomy Scissors FDA UDI
Generic Name
Corneal scissors, reusable FDA UDI
Device Name
Vannas Capsulotomy Scissors, Side Angled, Sharp Tips, 6mm Blds, Flat Handle FDA UDI
Model / Reference
AS12-033 FDA UDI
Description
Vannas Capsulotomy Scissors, Side Angled, Sharp Tips, 6mm Blds, Flat Handle FDA UDI

Identifiers

Catalog Number
AS12-033 FDA UDI
Primary DI / UDI-DI
08175700146036 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Corneal scissors, 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: Corneal scissors, reusable

Capsulotomy Scissors by Aurora Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f9e0edac-c261-4a0b-a9ab-9ef7165a59ac 35 fields · synced Jun 1, 2026