V. Mueller

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: Rigid endoscopic scissors, reusable FDA UDI
Device Name: V. Mueller THORACOSCOPIC DISSECTING SCIS 3.5CM BLADE, withBLUNT TIP, 5MM WORKING LENGTH 7.5 inches 19CM OVERALL LENGTH 13.5 inches 34CM FDA UDI
Model / Reference: CH2022 FDA UDI
Description: V. Mueller THORACOSCOPIC DISSECTING SCIS 3.5CM BLADE, withBLUNT TIP, 5MM WORKING LENGTH 7.5 inches 19CM OVERALL LENGTH 13.5 inches 34CM FDA UDI

Identifiers

Catalog Number: CH2022 FDA UDI
Primary DI / UDI-DI: 10885403181399 FDA UDI
FDA Product Code: GEI FDA UDI
GMDN Term: Rigid endoscopic scissors, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4400 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: Rigid endoscopic scissors, reusable

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

Similar devices

Also classified as Rigid endoscopic scissors, reusable.

Ambler Surgical — Ambler Surgical, LLC · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Arthrex® — Arthrex, Inc. · Class I
ELMED — ELMED INCORPORATED · Class II
Ambler Surgical — Ambler Surgical, LLC · Class II
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Olympus — Olympus Winter & Ibe GmbH · Class II
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

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

Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI e3716f5f-38b6-4824-abb2-0788831dd067 35 fields · synced Jun 8, 2026