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Eye Scissors

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
EYE SCISSORS FDA UDI
Generic Name
Enucleation scissors, reusable FDA UDI
Device Name
EYE SCISSORS STRAIGHT BLADE BEAD TIPS FDA UDI
Model / Reference
13-9334 FDA UDI
Description
EYE SCISSORS STRAIGHT BLADE BEAD TIPS FDA UDI

Identifiers

Catalog Number
13-9334 FDA UDI
Primary DI / UDI-DI
00192896015234 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Enucleation 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

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

Dimensions & Sizes

Size
Length — 4.25 Inch FDA UDI

Category: Enucleation scissors, reusable

Eye Scissors by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enucleation scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f4e784cb-3201-4dbf-a6b0-6d8eb69db1cb 36 fields · synced May 30, 2026