Urolift ®

FDA UDI

Class II (US FDA UDI)

by SCHÖLLY FIBEROPTIC GmbH

Identity

Trade Name: UROLIFT ® FDA UDI
Generic Name: Rigid endoscope working guide FDA UDI
Device Name: Working bridge with lockable working channel FDA UDI
Model / Reference: UL-WBRIDGE FDA UDI
Description: Working bridge with lockable working channel FDA UDI

Identifiers

Primary DI / UDI-DI: 04250480106624 FDA UDI
FDA Product Code: HIH FDA UDI
FAJ FDA UDI
GMDN Term: Rigid endoscope working guide FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.1690 FDA UDI
876.1500 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Rigid endoscope working guide

Urolift ® by SCHÖLLY FIBEROPTIC GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Rigid endoscope working guide.

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Olympus — Olympus Winter & Ibe GmbH · Class II
Urethrotome sheath only, 21Ch. — mahe medical gmbh · Class II
Olympus — Olympus Winter & Ibe GmbH · Class II
Olympus — Olympus Winter & Ibe GmbH · Class II
Resectoscopy working unit, passive, closed handle, 24/26/28.5Ch — mahe medical gmbh · 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 II	Pending data

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Manufacturer

Manufacturer: SCHÖLLY FIBEROPTIC GmbH

Sources (1)

FDA UDI dbdde3ec-2f13-4453-a769-fd3e59b74c68 35 fields · synced May 30, 2026