V. Mueller

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: Surgical retraction system, reusable FDA UDI
Device Name: V. Mueller Neuro/Spine SHADOW-LINE TOP-LOADING TRANSVERSE RETRACTOR FRAME DOUBLE HINGED, 200MM RACK FDA UDI
Model / Reference: S-0108 FDA UDI
Description: V. Mueller Neuro/Spine SHADOW-LINE TOP-LOADING TRANSVERSE RETRACTOR FRAME DOUBLE HINGED, 200MM RACK FDA UDI

Identifiers

Catalog Number: S0108 FDA UDI
Primary DI / UDI-DI: 10885403116063 FDA UDI
510(k) Number: K964402 FDA UDI
FDA Product Code: GZT FDA UDI
GMDN Term: Surgical retraction system, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4800 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

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

Similar devices

Also classified as Surgical retraction system, reusable.

45930R — Thompson Surgical Instruments, Inc. · Class IIa
Sigma — ALPHATEC SPINE, INC. · Class I
Omni-Tract® — Integra Lifesciences Corp. · Class I
Drills and Handpieces — SOUTHERN IMPLANTS (PTY) LTD · Class IIa
Thompson — Thompson Surgical Instruments · Class I
Nordent Manufacturing, Inc. — NORDENT MANUFACTURING INC · Class I
Thompson — Thompson Surgical Instruments · Class I
Thompson — Thompson Surgical Instruments · Class I

Cleared under the same submission

K964402 also covers:

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: Steris Corporation

Sources (1)

FDA UDI 5a082958-7a92-4054-b523-f2e88ffbf838 36 fields · synced Jun 8, 2026