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Series Oro-Nasal Masks

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 201603Model 6450; 7450 - Series Oro-Nasal MasksModel 6450; 7450 Series

by Hans Rudolph Inc

Identity

Trade Name
7450 RV2 MASK FDA UDI
Generic Name
Pulmonary function valve FDA UDI
Device Name
Series Oro-Nasal Masks EUDAMED
Oro-Nasal Mask EUDAMED
RV2 SMALL MASK BRACE SET FDA UDI
Model / Reference
6450; 7450 - Series Oro-Nasal Masks EUDAMED
201603 EUDAMED
6450; 7450 Series EUDAMED
7450 FDA UDI
Description
RV2 SMALL MASK BRACE SET FDA UDI

Identifiers

Catalog Number
201603 FDA UDI
Primary DI / UDI-DI
00874750004317 EUDAMEDFDA UDI
Basic UDI-DI
081713602691178BZ EUDAMED
Direct Marketing DI
00874750004317 EUDAMED
FDA Product Code
KGB FDA UDI
EMDN Code
R030199 RESPIRATORY MASKS - OTHER EUDAMED
GMDN Term
Pulmonary function valve FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5570 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia face mask, single-use

Series Oro-Nasal Masks by Hans Rudolph, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia face mask, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hans Rudolph Inc
EUDAMED SRN
US-MF-000004498
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (3)

  • EUDAMED 94a548e1-b1a2-40c4-88cd-cf8ff966c957 61 fields · synced Jun 19, 2026
  • FDA UDI 618072a1-1516-4e93-8b03-6838945ef6ef 34 fields · synced May 24, 2026
  • EUDAMED 8b5862d7-47b3-4dcf-8e03-2619395be97e 61 fields · synced Jun 19, 2026