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Westcott Conjunctival Scissors

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
WESTCOTT CONJUNCTIVAL SCISSORS FDA UDI
Generic Name
Conjunctival scissors, reusable FDA UDI
Device Name
WESTCOTT CONJUNCTIVAL SCISSORS LIGHT CURVED BLADE BLUNT TIP WIDE SERRATED HANDLE FDA UDI
Model / Reference
13-3301 FDA UDI
Description
WESTCOTT CONJUNCTIVAL SCISSORS LIGHT CURVED BLADE BLUNT TIP WIDE SERRATED HANDLE FDA UDI

Identifiers

Catalog Number
13-3301 FDA UDI
Primary DI / UDI-DI
00192896014473 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Conjunctival 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

Category: Conjunctival scissors, reusable

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

Similar devices

Also classified as Conjunctival scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI fe50c475-1898-4a93-9cfa-8070b9eb9f77 35 fields · synced May 30, 2026