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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Artery clamp FDA UDI
Device Name
COOLEY DILATOR #3 FDA UDI
Model / Reference
IPN006018 FDA UDI
Description
COOLEY DILATOR #3 FDA UDI

Identifiers

Catalog Number
355314 FDA UDI
Primary DI / UDI-DI
24026704522907 FDA UDI
FDA Product Code
DWP FDA UDI
GMDN Term
Artery clamp 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

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 — 116 Millimeter FDA UDI
Outer Diameter — 18.4 Millimeter FDA UDI

Category: Artery clamp

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

Similar devices

Also classified as Artery clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 74fb90b5-6d45-474e-8169-c52abf6d735d 36 fields · synced Jun 8, 2026