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Volume Calibration Syringe

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 113893Model 4900; 5510; 5520; 5530; 5540; 5550; 5570 Series

by Hans Rudolph Inc

Identity

Trade Name
5570 3L SYRINGE FDA UDI
Generic Name
Spirometer/pulmonary function analyser syringe FDA UDI
Device Name
Volume Calibration Syringe EUDAMED
5570 3L SYR NDD W/EASY-AIR ADAPTER FDA UDI
Model / Reference
4900; 5510; 5520; 5530; 5540; 5550; 5570 Series EUDAMED
113893 EUDAMED
5570 FDA UDI
Description
5570 3L SYR NDD W/EASY-AIR ADAPTER FDA UDI

Identifiers

Catalog Number
113893 FDA UDI
Primary DI / UDI-DI
00817136025728 EUDAMEDFDA UDI
Basic UDI-DI
081713602691184BU EUDAMED
FDA Product Code
BXW FDA UDI
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED
GMDN Term
Spirometer/pulmonary function analyser syringe FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.1870 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulmonary function analysis system, adult

Volume Calibration Syringe by Hans Rudolph, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hans Rudolph Inc
EUDAMED SRN
US-MF-000004498
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (2)

  • EUDAMED 9681a080-fe9a-4e80-8a9f-565c6f8d25e0 61 fields · synced Aug 3, 2026
  • FDA UDI bd082048-1408-4532-9243-60c8b12f4df9 34 fields · synced May 30, 2026