Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Corneal scissors, reusable FDA UDI
Device Name: CASTRO SCISSORS MINI ANGLED STAND FDA UDI
Model / Reference: IPN006728 FDA UDI
Description: CASTRO SCISSORS MINI ANGLED STAND FDA UDI

Identifiers

Catalog Number: 423340 FDA UDI
Primary DI / UDI-DI: 24026704526066 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 9.75 Centimeter FDA UDI

Category: Corneal scissors, reusable

Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
Stephens Instruments — KRISHNA IMPORTS INC · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Ophthalmic Scissors — Katena Products, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI d8790dcf-dcba-4e20-bc72-9f4eed079045 36 fields · synced May 30, 2026