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Organization name
UDI-DI code
Reference / catalog number

RCR1T-08-30 — Class IIa MDR by hestomed GmbH

MD Atlas
hestomed GmbH

EUDAMED last updated this device on Feb 6, 2026

RCR1T-08-30

426066638redox.remoteVA

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: hestomed GmbH
UDI-DI code: 04260666389802
Reference / catalog number: RCR1T-08-30

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Manufacturer information

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

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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		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260666389802
Basic UDI-DI: 426066638redox.remoteVA
Reference / catalog number: RCR1T-08-30
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