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Urolift ®

FDA UDI

Class II (US FDA UDI)

by SCHÖLLY FIBEROPTIC GmbH

Identity

Trade Name
UROLIFT ® FDA UDI
Generic Name
Luminal device flushing tubing set, reusable FDA UDI
Device Name
Tube Connector Luer Lock FDA UDI
Model / Reference
42.0472a FDA UDI
Description
Tube Connector Luer Lock FDA UDI

Identifiers

Primary DI / UDI-DI
04250480106532 FDA UDI
FDA Product Code
FAJ FDA UDI
HIH FDA UDI
GMDN Term
Luminal device flushing tubing set, reusable FDA UDI

Classification

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

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

Category: Luminal device flushing tubing set, reusable

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

Similar devices

Also classified as Luminal device flushing tubing set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SCHÖLLY FIBEROPTIC GmbH

Sources (1)

  • FDA UDI 6b4bf269-6ee4-45e1-8928-625c2f5f9aaa 35 fields · synced May 30, 2026