← Back to catalogue

2-Foot Double Loop Effort Belt

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 0523-2

by BRAEBON Medical Corporation

Identity

Trade Name
2-Foot Double Loop Effort Belt EUDAMED
BRAEBON 2-Foot Double Loop Effort Belt FDA UDI
Generic Name
Pneumograph FDA UDI
Device Name
Respiratory Effort Sensors EUDAMED
Belt for use with PVDF Respiratory effort sensor.. FDA UDI
Model / Reference
0523-2 EUDAMEDFDA UDI
Description
Belt for use with PVDF Respiratory effort sensor.. FDA UDI

Identifiers

Catalog Number
0523-2 FDA UDI
Primary DI / UDI-DI
B140052320 EUDAMEDFDA UDI
Basic UDI-DI
++B140EffortFU EUDAMED
510(k) Number
K982216 FDA UDI
FDA Product Code
BZQ FDA UDI
EMDN Code
Z12100585 POLYSOMNOGRAPHY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Pneumograph 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 — 2 Feet FDA UDI

2-Foot Double Loop Effort Belt 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 5409ea58-3163-463b-9e98-0a512c902ffd 61 fields · synced Aug 3, 2026
  • FDA UDI 4a66f7cd-4751-43a6-8f56-6ddb5eba2f8e 37 fields · synced May 30, 2026