V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: General-purpose surgical spatula FDA UDI
Device Name: V. Mueller CASTROVIEJO CYCLODIALYSIS SPATULA, DOUBLE-ENDED 1CM X 0.25MM and 1.5CM X 0.25MM OVERALL LENGTH 5 inches 12.7CM FDA UDI
Model / Reference: OP2052 FDA UDI
Description: V. Mueller CASTROVIEJO CYCLODIALYSIS SPATULA, DOUBLE-ENDED 1CM X 0.25MM and 1.5CM X 0.25MM OVERALL LENGTH 5 inches 12.7CM FDA UDI

Identifiers

Catalog Number: OP2052 FDA UDI
Primary DI / UDI-DI: 10885403097164 FDA UDI
FDA Product Code: HND FDA UDI
GMDN Term: General-purpose surgical spatula FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 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: General-purpose surgical spatula

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

Similar devices

Also classified as General-purpose surgical spatula.

Fisherbrand — FISHER SCIENTIFIC COMPANY L.L.C. · Class I
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Sklar® — Sklar Corporation · Class I
ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. · Class I
Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC · Class I
Bausch + Lomb — Bausch & Lomb Incorporated · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
MicroFrance® — Integra Microfrance · 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 931c7484-949c-45b3-bfbf-f38ec99298b4 35 fields · synced Jun 8, 2026