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Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
LIGHTCARRIER FOR 52-2190 OSSOFF PILLING FDA UDI
Model / Reference
IPN008814 FDA UDI
Description
LIGHTCARRIER FOR 52-2190 OSSOFF PILLING FDA UDI

Identifiers

Catalog Number
527864 FDA UDI
Primary DI / UDI-DI
14026704722201 FDA UDI
FDA Product Code
EQH FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4350 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

Dimensions & Sizes

Size
Length — 5.44 Inch FDA UDI
Width — 4.9 Inch FDA UDI
Depth — 0.42 Inch FDA UDI

Category: Fibreoptic light cable

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

Similar devices

Also classified as Fibreoptic light cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 79569b88-9f1d-41aa-ad4c-7867b566c998 36 fields · synced May 30, 2026