Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

RCR1T-08-15 — Class IIa MDR by hestomed GmbH

MD Atlas
hestomed GmbH

EUDAMED last updated this device on Feb 6, 2026

RCR1T-08-15

426066638redox.remoteVA

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: hestomed GmbH
UDI-DI code: 04260666389833
Reference / catalog number: RCR1T-08-15

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: hestomed GmbH
SRN: DE-MF-000006850
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW999
enthält Blei

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 1, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260666389833
Basic UDI-DI: 426066638redox.remoteVA
Reference / catalog number: RCR1T-08-15
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A030104FLOW REGULATORS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

G10 064409 0012Issued
Quality management systemNotified body: 0123Expiry: Dec 21, 2028

Related devices

compact flowmeter redox. click 0-15 L426066638redox.clickUAOn the market compact flowmeter redox. click 0-15 L426066638redox.clickUAOn the market compact flowmeter redox. click 0-15 L426066638redox.clickUAOn the market compact flowmeter redox. click 0-15 L; G1/4"a for assembly426066638redox.clickUAOn the market

compact flowmeter redox. click 0-15 L; G1/4"a for assembly

426066638redox.clickUA

On the market