V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: Nerve/vessel retractor FDA UDI
Device Name: RHOTON HOOK ANGLED 90DEG BLUNT OVERALL LENGTH 7-1/2 inches19.1CM FDA UDI
Model / Reference: NL3785-010 FDA UDI
Description: RHOTON HOOK ANGLED 90DEG BLUNT OVERALL LENGTH 7-1/2 inches19.1CM FDA UDI

Identifiers

Catalog Number: NL3785010 FDA UDI
Primary DI / UDI-DI: 10885403073656 FDA UDI
FDA Product Code: GZX FDA UDI
GMDN Term: Nerve/vessel retractor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4525 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Nerve/vessel retractor

V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nerve/vessel retractor.

Ambler Surgical — Ambler Surgical, LLC · Class I
BOSS Instruments — Boss Instruments, Ltd. · Class I
Life Instruments — Life Instrument Corporation · Class I
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
JACOBSON SHEPARDS HOOK PROBE — SONTEC INSTRUMENTS, INC. · Class I
Avalign — AVALIGN TECHNOLOGIES, Inc. · Class I
Integra® Ruggles®-Redmond™ — Integra LifeSciences Production Corporation · Class I
RAVINE Lateral Access System — K2M, INC. · Class I

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI 879f9675-e9cc-4500-ae65-98ed451655bf 35 fields · synced Jun 8, 2026