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Ultima Nasal Cannula, Pediatric

EUDAMED

Class I (EU MDR)

Ref 8582PED

by BRAEBON Medical Corporation

Identity

Trade Name
Ultima Nasal Cannula, Pediatric EUDAMED
Device Name
Airflow Cannula EUDAMED
Model / Reference
8582PED EUDAMED

Identifiers

Primary DI / UDI-DI
B1408582PED0 EUDAMED
Basic UDI-DI
++B140CannulaPD EUDAMED
EMDN Code
Z12100585 POLYSOMNOGRAPHY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Ultima Nasal Cannula, Pediatric by Braebon Medical Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CA-MF-000002190
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED 2510b2dc-c0d4-4e98-a4ff-75e82c0fcc57 61 fields · synced Oct 6, 2026