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Accutron Inc.

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 33034-10-CAPModel Nasal Hood

by Accutron

Identity

Trade Name
Accutron Inc. EUDAMED
ClearView Nasal Mask and Capnography Bundle – Large Adult Outlaw Orange (pkg.12) FDA UDI
Generic Name
Anaesthesia face mask, single-use FDA UDI
Device Name
ClearView Nasal Mask and Capnography Bundle – Large Adult Outlaw Orange (pkg. of 12) FDA UDI
Model / Reference
Nasal Hood EUDAMED
33034-10-CAP EUDAMEDFDA UDI
Description
ClearView Nasal Mask and Capnography Bundle – Large Adult Outlaw Orange (pkg. of 12) FDA UDI

Identifiers

Catalog Number
33034-10-CAP FDA UDI
Primary DI / UDI-DI
00813830028676 EUDAMEDFDA UDI
Basic UDI-DI
B-00813830028676 EUDAMED
FDA Product Code
KHA FDA UDI
EMDN Code
R03010101 ANAESTHETIC FACE MASKS EUDAMED
GMDN Term
Anaesthesia face mask, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5590 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia face mask, single-use

Accutron Inc. by Accutron — Class IIa — MDD, 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/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accutron
EUDAMED SRN
US-MF-000009363
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED e6bd0e37-a24f-4a1e-9048-6e8efb744a7e 61 fields · synced Jul 14, 2026
  • FDA UDI b48557bd-60ac-4045-9f39-70209096cca8 34 fields · synced May 30, 2026