← Back to catalogue

Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Urethral sound, reusable FDA UDI
Device Name
VAN BUREN SOUND 16 FRENCH 10 5/8", 26.99 CENTIMETER FDA UDI
Model / Reference
IPN004640 FDA UDI
Description
VAN BUREN SOUND 16 FRENCH 10 5/8", 26.99 CENTIMETER FDA UDI

Identifiers

Catalog Number
241116 FDA UDI
Primary DI / UDI-DI
24026704515169 FDA UDI
FDA Product Code
FBX FDA UDI
GMDN Term
Urethral sound, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5520 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 275 Millimeter FDA UDI

Category: Urethral sound, reusable

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

Similar devices

Also classified as Urethral sound, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 7370e98c-5684-4738-8200-b5fdc5fc04cb 36 fields · synced May 31, 2026