← Back to catalogue

Breathing Reservoir Bag (Test Lung)

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref G-118000-0-NPModel G-118000-0

by VADI Medical Technology Co., Ltd.

Identity

Trade Name
VADI MEDICAL FDA UDI
Generic Name
Lung physical simulator FDA UDI
Device Name
Breathing Reservoir Bag (Test Lung) EUDAMEDFDA UDI
Model / Reference
G-118000-0 EUDAMEDFDA UDI
G-118000-0-NP EUDAMED
Description
Breathing Reservoir Bag (Test Lung) FDA UDI

Identifiers

Catalog Number
G-118000-0-NP FDA UDI
Primary DI / UDI-DI
04719875340031 EUDAMEDFDA UDI
Basic UDI-DI
B-04719875340031 EUDAMED
FDA Product Code
BTC FDA UDI
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED
GMDN Term
Lung physical simulator FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.5320 FDA UDI
Market of Registration
Austria 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Pulmonary function analysis system, adult

Breathing Reservoir Bag (Test Lung) by VADI Medical Technology Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
TW-MF-000022930
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (2)

  • EUDAMED e5d3e55f-6734-41c5-a094-7687ed4f0419 61 fields · synced Jun 19, 2026
  • FDA UDI c9437ca6-2fd7-49e8-9dae-5bd07d3d4239 34 fields · synced May 30, 2026