Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Irrigation syringe FDA UDI
Device Name: ABRAHAM CANNULA LUER LOCK FDA UDI
Model / Reference: IPN007974 FDA UDI
Description: ABRAHAM CANNULA LUER LOCK FDA UDI

Identifiers

Catalog Number: 507434 FDA UDI
Primary DI / UDI-DI: 24026704532166 FDA UDI
FDA Product Code: KYZ FDA UDI
GMDN Term: Irrigation syringe FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6960 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 — 150 Millimeter FDA UDI

Category: Irrigation syringe

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

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Medline — MEDLINE INDUSTRIES, INC. · Class I
PROBEVAC — PLASDENT CORP. · Class I
HSW HENKE-JECT® — Henke-Sass, Wolf GmbH · Class II
Monoject — Cardinalhealth · 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 77a48fc6-ed9c-47f0-8343-6afd45004b44 36 fields · synced May 30, 2026