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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Urethral sound, reusable FDA UDI
Device Name
SCHROEDER FORCEPS STRAIGHT 9 3/8", 23.81CM FDA UDI
Model / Reference
IPN004500 FDA UDI
Description
SCHROEDER FORCEPS STRAIGHT 9 3/8", 23.81CM FDA UDI

Identifiers

Catalog Number
213180 FDA UDI
Primary DI / UDI-DI
24026704514919 FDA UDI
FDA Product Code
HDC FDA UDI
GMDN Term
Urethral sound, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 252 Millimeter FDA UDI

Category: Urethral sound, reusable

Pilling by Teleflex Incorporated — Class II — 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

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI d4bcec7a-62ab-4bc8-969a-8a9eb7096087 36 fields · synced Jun 8, 2026