Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Centrally-inserted central venous catheter FDA UDI
Device Name: FITCH OBTURATOR 26 FRENCH FDA UDI
Model / Reference: IPN005339 FDA UDI
Description: FITCH OBTURATOR 26 FRENCH FDA UDI

Identifiers

Catalog Number: 351316 FDA UDI
Primary DI / UDI-DI: 24026704517019 FDA UDI
FDA Product Code: DWS FDA UDI
GMDN Term: Centrally-inserted central venous catheter FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 870.4500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

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 — 17.875 Inch FDA UDI

Category: Centrally-inserted central venous catheter

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

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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 018607f3-7c0e-4ef0-b338-1adc209b248d 36 fields · synced May 29, 2026