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Organization name
UDI-DI code
Reference / catalog number

Micropure-S-B — Class IIa MDR by Allmed Medical GmbH

MD Atlas
Allmed Medical GmbH

EUDAMED last updated this device on May 20, 2026

Micropure-S-B

426015772MICROPUREEO5J

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Allmed Medical GmbH
UDI-DI code: 04260157724334
Reference / catalog number: Micropure-S-B

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Manufacturer information

Organization name: Allmed Medical GmbH
SRN: DE-MF-000007862
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Contraindications: - Avoid use of the MicroPure-S made of Polysulfone membrane in patients with known hypersensitivity. - Patients with sensitivity to ETO should not be exposed to Allmed Micropure.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Feb 3, 2016	Dec 20, 2019
EL	Jan 4, 2019	Dec 19, 2019

Device identification

Trade name: not provided
UDI-DI code: 04260157724334
Basic UDI-DI: 426015772MICROPUREEO5J
Reference / catalog number: Micropure-S-B
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: Allmed MicroPure-S is intended to be used for purification of ultrapure dialysis fluid to produce on-line preparation of sterile substitution fluid. Purification is achieved through the high bacterial and endotoxin retention capabilities of the filter. Ethylene oxide (EO) sterilized, Intended to be connected with BELLCO machine (BELLCO Formula 2000)
Additional information URL: https://allmedgroup.com/e-ifu-repository/
Clinical sizes: 0.2 MU85

EMDN nomenclature code(s)

F01080201ENDOTOXIN REMOVAL FILTERS

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

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.