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V. Mueller

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
V. Mueller TITANIUM BAYONET BIPOLAR FRCP IRRIGATING, STRT, INSULATED 1.5MM TIP, SQUARE GRIP HANDLE OVERALL LENGTH 8-3/4 inches 222MM FDA UDI
Model / Reference
F-5301 FDA UDI
Description
V. Mueller TITANIUM BAYONET BIPOLAR FRCP IRRIGATING, STRT, INSULATED 1.5MM TIP, SQUARE GRIP HANDLE OVERALL LENGTH 8-3/4 inches 222MM FDA UDI

Identifiers

Catalog Number
F5301 FDA UDI
Primary DI / UDI-DI
10885403041266 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, bipolar, 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 7ee0fcd4-7fef-4cab-83a9-6a81e33a28bf 35 fields · synced Jun 8, 2026