Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Vascular dilator, reusable FDA UDI
Device Name: GARRETT DILATOR 3MM 14CM FDA UDI
Model / Reference: IPN005961 FDA UDI
Description: GARRETT DILATOR 3MM 14CM FDA UDI

Identifiers

Catalog Number: 355084 FDA UDI
Primary DI / UDI-DI: 24026704522365 FDA UDI
FDA Product Code: DWP FDA UDI
GMDN Term: Vascular dilator, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4475 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Length — 5.5 Inch FDA UDI
Outer Diameter — 3 Millimeter FDA UDI

Category: Vascular dilator, reusable

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

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Marina Medical — MARINA MEDICAL INSTRUMENTS, 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 II	Pending data

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Manufacturer

Manufacturer: Teleflex Incorporated

Sources (1)

FDA UDI a5595f8d-a85c-40fd-856b-8c61137c7dd9 36 fields · synced May 31, 2026