Urolift ®

FDA UDI

Class II (US FDA UDI)

by SCHÖLLY FIBEROPTIC GmbH

Identity

Trade Name: UROLIFT ® FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: Grasping forceps, 7 Fr. x 400 mm FDA UDI
Model / Reference: UL-GRASP FDA UDI
Description: Grasping forceps, 7 Fr. x 400 mm FDA UDI

Identifiers

Primary DI / UDI-DI: 04250480106631 FDA UDI
FDA Product Code: HIH FDA UDI
FAJ FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, reusable 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 endoscopic biopsy forceps, reusable

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

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Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
ELMED — ELMED INCORPORATED · 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 477a2158-04e9-4624-a95f-d30dcd181b0e 36 fields · synced May 30, 2026