Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name: PILLING FDA UDI
Generic Name: Head-worn fibreoptic light FDA UDI
Device Name: Headlight Var 10-75mm Spot w/9' Bif Cabl FDA UDI
Model / Reference: IPN920536 FDA UDI
Description: Headlight Var 10-75mm Spot w/9' Bif Cabl FDA UDI

Identifiers

Catalog Number: 528339PS FDA UDI
Primary DI / UDI-DI: 14026704737168 FDA UDI
FDA Product Code: EBA FDA UDI
GMDN Term: Head-worn fibreoptic light FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4630 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Head-worn fibreoptic light

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

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ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. · Class II
90 Deg Fiber Optic HL — Medical Illumination International, Inc · Class II
BR Surgical, LLC — BR SURGICAL LLC · Class II
Surgical Headlight — GULF FIBEROPTICS, INC. · Class II

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 23e3e967-e483-404e-bd9a-5efcaf655c4d 35 fields · synced May 30, 2026