V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name: V. Mueller FDA UDI
Generic Name: Nasal file/rasp FDA UDI
Device Name: FOMON NASAL RASP FINE TEETH DOWNCUT EACH BLADE 4.2X0.7CM OVERALL LENGTH 8-1/2 inches22CM FDA UDI
Model / Reference: RH2010-001 FDA UDI
Description: FOMON NASAL RASP FINE TEETH DOWNCUT EACH BLADE 4.2X0.7CM OVERALL LENGTH 8-1/2 inches22CM FDA UDI

Identifiers

Catalog Number: RH2010001 FDA UDI
Primary DI / UDI-DI: 10885403113710 FDA UDI
FDA Product Code: KBA FDA UDI
GMDN Term: Nasal file/rasp FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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: Nasal file/rasp

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

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HNM MEDICAL — HNM STAINLESS, LLC. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · 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

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Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI d39bc722-4c12-446b-a68b-51fb908604a7 35 fields · synced Jun 8, 2026