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Connector Cables

EUDAMEDFDA UDI

Class I (EU MDR)

Ref DUAL KEYHOLE CONNECTOR TO 3.5 mm FEMALE PHONE CONNECTOR CABLE

by BRAEBON Medical Corporation

Identity

Trade Name
BRAEBON 1 mm Dual Safety Pin to 3.5 mm Female Phone Connector Cable FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Connector Cables EUDAMED
Cable for connecting sensors to a device. FDA UDI
Model / Reference
DUAL KEYHOLE CONNECTOR TO 3.5 mm FEMALE PHONE CONNECTOR CABLE EUDAMED
0354 FDA UDI
Description
Cable for connecting sensors to a device. FDA UDI

Identifiers

Catalog Number
0354 FDA UDI
Primary DI / UDI-DI
B14003540 EUDAMEDFDA UDI
Basic UDI-DI
++B140ConnectSW EUDAMED
Direct Marketing DI
B14003540 EUDAMED
510(k) Number
K001743 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
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 18 Inch FDA UDI

Connector Cables 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

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Manufacturer

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

Sources (2)

  • EUDAMED 157c036c-0df1-4f96-8961-5982bb83f012 61 fields · synced Oct 7, 2026
  • FDA UDI 0c923889-2c84-4fdd-ad70-5a2d0bcbbd0e 38 fields · synced May 29, 2026