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Interface Cable for Alice 6

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 0376Model 0303

by BRAEBON Medical Corporation

Identity

Trade Name
Interface Cable for Alice 6 EUDAMED
BRAEBON Interface Cable for Alice 6 FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Male to Male Luer Adapter EUDAMED
Cable for connecting sensors to a device. FDA UDI
Model / Reference
0303 EUDAMED
0376 EUDAMEDFDA UDI
Description
Cable for connecting sensors to a device. FDA UDI

Identifiers

Catalog Number
0376 FDA UDI
Primary DI / UDI-DI
B14003760 EUDAMEDFDA UDI
Basic UDI-DI
++B140Connector4X EUDAMED
Direct Marketing DI
B14003760 EUDAMED
510(k) Number
K984431 FDA UDI
FDA Product Code
BZQ FDA UDI
EMDN Code
Z12100580 POLYSOMNOGRAPHY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Market of Registration
France 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Interface Cable for Alice 6 by Braebon Medical Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 494a564c-0bac-4d31-b178-98ff1a36944e 61 fields · synced Oct 6, 2026
  • FDA UDI 3c2e2a5a-5cdd-4ec9-bba1-b0ebf179abe5 37 fields · synced May 30, 2026